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)K233688Substantially equivalent (SESE) · 2023-12-13clearance family
- De NovoDEN220039De Novo granted (DENG) · 2023-03-08 · +1 earlier decisionsclearance family
Predicate lineage
- K233688
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 |
|---|---|---|---|---|
| 2021-08-03 | NAI | No action indicated | Quidel Corporation | 0 |
| 2018-01-29 | VAI | Voluntary action indicated | Quidel Corporation | 5 |
| 2017-04-10 | VAI | Voluntary action indicated | Quidel Corporation | 0 |
| 2014-01-13 | NAI | No action indicated | Quidel Corporation | 0 |
| 2013-05-21 | NAI | No action indicated | Quidel Corporation | 0 |
| 2013-01-17 | VAI | Voluntary action indicated | Quidel Corporation | 1 |
| 2011-03-16 | NAI | No action indicated | Quidel Corporation | 0 |
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