510(k) K042338 ยท DQX Wire, Guide, Catheter
CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Sep 16, 2004 |
| Received | Aug 30, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042338
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.