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HP 400 series type monitor cable
Model 70320 · TRUER MEDICAL, INC. · DI 00859290006366
IKD — Cable, Electrode · Class II · 21 CFR 890.1175
UDILibrary device dossier · generated 2026-09-11 · 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.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-03
0
1
2019-04
0
1
2019-06
0
1
2019-07
0
1
2019-08
0
3
2019-09
0
1
2020-01
0
1
2020-02
0
2
2020-03
0
1.5
2020-05
0
1
2020-06
0
1.5
2020-08
0
1
2020-09
0
3
2020-11
0
1
2021-01
0
1
2021-02
0
1
2021-03
0
1
2021-04
0
1
2021-06
0
1.5
2021-07
0
1
2021-08
0
3
2021-11
0
1
2022-05
0
1
2022-06
0
2.8
2022-07
0
3
2022-08
0
1.5
2022-12
0
1
2023-03
0
1.5
2023-08
0
1.17
2023-10
0
1
2023-11
0
3
2024-01
0
1
2024-03
0
1
2024-04
0
2
2024-05
0
1
2024-06
0
1
2024-11
0
2
2025-02
0
1
2025-04
0
1.5
2025-06
0
1.67
2025-07
0
3.5
2025-08
0
2.33
2025-09
0
1.5
2025-10
0
3.5
2025-11
0
3
2025-12
0
3
2026-01
0
2
2026-02
0
5
2026-03
0
2.2
2026-04
0
3
2026-05
0
2.14
2026-06
0
2.5
This device (reports/month)Average device in IKD (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — TRUER MEDICAL, INC.