510(k) K884481 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE
| Applicant | Mallinckroot, Inc., St Louis MO, US |
| Decision | Substantially Equivalent, Jan 10, 1989 |
| Received | Oct 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884481
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.