DOUBLE RING ARRAY
Model 07098002 · Siemens Healthcare GmbH · DI 04056869014142
LNH — System, Nuclear Magnetic Resonance Imaging · Class II · 21 CFR 892.1000
LNI — System, Nuclear Magnetic Resonance Spectroscopic · Class II · 21 CFR 892.1000
MOS — Coil, Magnetic Resonance, Specialty · Class II · 21 CFR 892.1000
UDILibrary device dossier · generated 2026-09-07 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-02 | 0 | 1 |
| 2019-03 | 0 | 2.29 |
| 2019-04 | 0 | 3.05 |
| 2019-05 | 0 | 1 |
| 2019-06 | 0 | 1 |
| 2019-07 | 0 | 2.13 |
| 2019-10 | 0 | 1.42 |
| 2019-11 | 0 | 1 |
| 2019-12 | 0 | 1 |
| 2020-02 | 0 | 1 |
| 2020-03 | 0 | 1.25 |
| 2020-07 | 0 | 1.69 |
| 2020-08 | 0 | 4 |
| 2020-09 | 0 | 1 |
| 2020-10 | 0 | 1 |
| 2020-12 | 0 | 1.36 |
| 2021-01 | 0 | 1 |
| 2021-02 | 0 | 1 |
| 2021-03 | 0 | 1 |
| 2021-04 | 0 | 3 |
| 2021-05 | 0 | 1 |
| 2021-07 | 0 | 1 |
| 2021-08 | 0 | 1 |
| 2021-09 | 0 | 1.29 |
| 2021-10 | 0 | 1.38 |
| 2021-11 | 0 | 1 |
| 2021-12 | 0 | 1 |
| 2022-01 | 0 | 1 |
| 2022-02 | 0 | 1.43 |
| 2022-03 | 0 | 1.14 |
| 2022-04 | 0 | 1 |
| 2022-05 | 0 | 1 |
| 2022-06 | 0 | 1.29 |
| 2022-07 | 0 | 1 |
| 2022-08 | 0 | 1 |
| 2022-09 | 0 | 1.33 |
| 2022-10 | 0 | 1.2 |
| 2022-11 | 0 | 1 |
| 2022-12 | 0 | 1.31 |
| 2023-01 | 0 | 1 |
| 2023-02 | 0 | 1.25 |
| 2023-03 | 0 | 2.81 |
| 2023-04 | 0 | 1.57 |
| 2023-05 | 0 | 1.77 |
| 2023-06 | 0 | 1.43 |
| 2023-07 | 0 | 1.39 |
| 2023-08 | 0 | 2.33 |
| 2023-09 | 0 | 2 |
| 2023-10 | 0 | 1.79 |
| 2023-11 | 0 | 2.22 |
| 2023-12 | 0 | 1.17 |
| 2024-01 | 0 | 1.17 |
| 2024-02 | 0 | 1 |
| 2024-03 | 0 | 1.25 |
| 2024-04 | 0 | 1.25 |
| 2024-05 | 0 | 1 |
| 2024-06 | 0 | 1 |
| 2024-07 | 0 | 1.4 |
| 2024-08 | 0 | 1.69 |
| 2024-09 | 0 | 1.25 |
| 2024-10 | 0 | 1.33 |
| 2024-11 | 0 | 1.89 |
| 2024-12 | 0 | 1.22 |
| 2025-01 | 0 | 4.67 |
| 2025-02 | 0 | 3.29 |
| 2025-03 | 0 | 2.41 |
| 2025-04 | 0 | 2 |
| 2025-05 | 0 | 2.36 |
| 2025-06 | 0 | 4.95 |
| 2025-07 | 0 | 5.46 |
| 2025-08 | 0 | 7.53 |
| 2025-09 | 0 | 4.34 |
| 2025-10 | 0 | 5.1 |
| 2025-11 | 0 | 3.92 |
| 2025-12 | 0 | 7 |
| 2026-01 | 0 | 6.47 |
| 2026-02 | 0 | 3.8 |
| 2026-03 | 0 | 3.44 |
| 2026-04 | 0 | 3.62 |
| 2026-05 | 0 | 6.38 |
| 2026-06 | 0 | 3 |
Regulatory clearances
- None linked in the loaded window.
Predicate lineage
K121434 — cites (transitively): K082427 (d1), K091114 (d1), K103274 (d1), K053042 (d2) — cited as predicate by K123510, K123920, K123938, K130262, K130749, K132831, K132951, K133692, K140666, K141977, K143020, K152602, K163234, K170396, K170840, K181613, K191050, K220018
K123938 — cites (transitively): K082427 (d1), K121434 (d1), K091114 (d2), K103274 (d2), K053042 (d3) — cited as predicate by K132119, K133226, K170840
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — Siemens Healthcare GmbH
- NAI 2014-09-25 Siemens AG/Siemens Healthcare GmbH · 0 citations
- VAI 2011-06-09 Siemens Healthcare GmbH · 1 citations
- NAI 2010-09-14 Siemens AG/Siemens Healthcare GmbH · 0 citations