510(k) K960832 ยท MJN Catheter, Intravascular Occluding, Temporary
OCCLUSION BALLOON CATHETER
| Applicant | Interventional Therapeutics Corp., Fremont CA, US |
| Decision | Substantially Equivalent, May 29, 1996 |
| Received | Feb 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960832
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.