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VISUALASE
MEDTRONIC NAVIGATION, INC. · Model 9735542 · UDI-DI 00763000521370
1
510(k) clearances
1
Adverse events
1
Recalls
7
Facilities
Description
SYSTEM 9735542 15W VISUALASE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-10-14 | Medtronic Navigation, Inc. | Due to a defect in the outer pouch sterile seal |
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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.