510(k) K981061 ยท GCC Dilator, Catheter
INTRAVASCULAR RETRIEVAL DEVICE
| Applicant | Med Institute, Inc., West Lafayette IN, US |
| Decision | Substantially Equivalent, May 26, 1998 |
| Received | Mar 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981061
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.