510(k) K994141 ยท MJN Catheter, Intravascular Occluding, Temporary
CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510; WIRE, GUIDE, CATHETER, MODEL QSW1000
| Applicant | Medtronic Ave, Inc., Santa Rosa CA, US |
| Decision | Substantially Equivalent, Jul 21, 2000 |
| Received | Dec 8, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994141
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.