510(k) K970668 ยท DQY Catheter, Percutaneous
THE AMPLANTZ GOOSE NECK MICROSNARE
| Applicant | Microvena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, Jun 10, 1998 |
| Received | Feb 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970668
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.