510(k) K993436 ยท FGM Probe And Director, Gastro-Urology
CAVERMAP SURGICAL AID
| Applicant | Uromed Corp., Norwood MA, US |
| Decision | Substantially Equivalent, Feb 11, 2000 |
| Received | Oct 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993436
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 13, 2003 | Blue Torch Medical Technologies CaverMap Surgical Aid Disposable Kit with Focused Probe Tip, Sterile
Part Number: 8305 Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.