510(k) K992320 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MEGABELLO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER
| Applicant | Boston Scientific Corp, Plymouth MN, US |
| Decision | Substantially Equivalent, May 18, 2000 |
| Received | Jul 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992320
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.