510(k) K911215 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
GESCO PER-Q-CATH NEEDLE
| Applicant | Gesco Intl., Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Jun 6, 1991 |
| Received | Mar 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911215
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.