510(k) K905639 ยท DQX Wire, Guide, Catheter
TORQUE HANDLE DEVICE FOR GUIDEWIRE
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Feb 20, 1991 |
| Received | Dec 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905639
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.