510(k) K082922 ยท DQX Wire, Guide, Catheter
FREEWAY AND RAILRUNNER GUIDEWIRES
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Dec 9, 2008 |
| Received | Oct 1, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082922
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.