510(k) K921856 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.
| Applicant | Schneider Intl., Ltd., Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 21, 1992 |
| Received | Apr 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921856
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.