510(k) K903606 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
GUIDEWIRE TORQUE DEVICE AND GUIDEWIRE INTRODUCER
| Applicant | North American Instrument Corp., Glens Falls NY, US |
| Decision | Substantially Equivalent, Sep 27, 1990 |
| Received | Jul 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903606
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.