510(k) K896108 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
THE PILOT SCIMED TORQUE DEVICE
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jan 9, 1990 |
| Received | Oct 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896108
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.