510(k) K880158 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ANGIOPLASTY BALLOON INFLATION DEVICE
| Applicant | L.O.N. Research, Inc., Sanford FL, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Jan 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880158
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.