Adverse-event reports (MAUDE)
Read this first: 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 shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
- 510(k)K173063Substantially equivalent (SESE) · 2017-10-23clearance family
Predicate lineage
Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2022-02-28 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2022-02-28 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2019-03-04 | VAI | Voluntary action indicated | Acist Medical Systems | 1 |
| 2019-03-04 | VAI | Voluntary action indicated | Acist Medical Systems | 1 |
| 2016-03-01 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2016-03-01 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2012-06-06 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2012-06-06 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2010-03-24 | NAI | No action indicated | Acist Medical Systems | 0 |
| 2010-03-24 | NAI | No action indicated | Acist Medical Systems | 0 |
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