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"Skytron 10"" rear rail"
Model H8-300-07 · SKYTRON LLC · DI 10841736114930
FQO — Table, Operating-Room, Ac-Powered · Class I · 21 CFR 878.4960
UDILibrary device dossier · generated 2026-09-06 · 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)
2020-01
0
2
2020-03
0
1
2020-09
0
4
2020-10
0
4
2020-11
0
16
2020-12
0
8
2021-01
0
1
2021-02
0
16
2021-03
0
24
2021-04
0
5.33
2021-06
0
4
2021-07
0
4
2021-08
0
1
2021-10
0
1
2021-11
0
1
2021-12
0
1
2022-01
0
1
2022-02
0
5.67
2022-03
0
1
2022-04
0
1
2022-05
0
1.33
2022-06
0
1
2022-07
0
1.33
2022-08
0
1.4
2022-09
0
2.67
2022-10
0
1.17
2022-11
0
1
2022-12
0
1.2
2023-01
0
1.25
2023-02
0
1.14
2023-03
0
1.5
2023-04
0
1.29
2023-05
0
1.13
2023-06
0
1.08
2023-07
0
2.22
2023-08
0
1.75
2023-09
0
3.17
2023-10
0
1.68
2023-11
0
1.64
2023-12
0
2.78
2024-01
0
3.33
2024-02
0
2.33
2024-03
0
1.64
2024-04
0
1.64
2024-05
0
1.57
2024-06
0
1.71
2024-07
0
1.33
2024-08
0
1.89
2024-09
0
1.5
2024-10
0
2.17
2024-11
0
2
2024-12
0
1.67
2025-01
0
1.27
2025-02
0
2.31
2025-03
0
2
2025-04
0
1.4
2025-05
0
2.85
2025-06
0
2.67
2025-07
0
2
2025-08
0
1.67
2025-09
0
2.4
2025-10
0
1.75
2025-11
0
2.25
2025-12
0
2
2026-01
0
1.9
2026-02
0
2.11
2026-03
0
22.5
2026-04
0
2
2026-05
0
2.33
2026-06
0
2.11
This device (reports/month)Average device in FQO (reports/device/month)