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VACU-TEC S.C.
DIESSE DIAGNOSTICA SENESE SPA · Model 10600 · UDI-DI 08033891321086
1
510(k) clearances
32
Adverse events
1
Recalls
17
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-04-12 | Vital Diagnostics, Inc. | The tube may fall out or separate from the Slider adapter |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.