510(k) K920547 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ULTRA-THIN
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, May 6, 1992 |
| Received | Feb 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920547
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.