510(k) K924358 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ACCEMT DG(TM) BALLOON ANGIOPLASTY CATH, MODIFIED
| Applicant | Cook, Inc., Bloomington IN, US |
| Decision | Substantially Equivalent, May 20, 1993 |
| Received | Aug 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924358
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.