510(k) K915895 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
STEALTH DILATION CATHETER SYSTEM (MODIFIED)
| Applicant | Target Therapeutics, San Jose CA, US |
| Decision | Substantially Equivalent, Jun 4, 1992 |
| Received | Jul 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915895
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.