510(k) K022813 ยท DQX Wire, Guide, Catheter
STEERABLE GUIDEWIRE
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Feb 14, 2003 |
| Received | Aug 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022813
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.