510(k) K897106 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MEDI-TECH DILATATION CATHETERS ULTRA THIN II
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Oct 16, 1990 |
| Received | Dec 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897106
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.