510(k) K972065 ยท DQY Catheter, Percutaneous
AURORA
| Applicant | Neurovena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, Jan 27, 1999 |
| Received | Jun 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972065
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.