Home › Ventana Medical Systems, Inc. › HPV FAMILY 6 SYSTEM CONTROL SLIDES [B]
HPV FAMILY 6 SYSTEM CONTROL SLIDES [B]
Ventana Medical Systems, Inc. · Model 05273528001 · UDI-DI 04015630971909
10
510(k) clearances
1
Adverse events
1
Recalls
7
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-01-21 | Diagnostic Hybrids Inc | During QC post release monitoring, the firm determined that the monolayer culture of rabbit kidney cells previously distributed by the firm, appeared to contain another type of cel |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
