510(k) K901601 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
HOLLOW MOTOR DRIVE UNIT
| Applicant | Devices For Vascular Intervention, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Jul 6, 1990 |
| Received | Apr 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901601
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.