510(k) K896403 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM
| Applicant | Intensive Technology, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 6, 1990 |
| Received | Nov 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896403
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.