510(k) K921200 ยท KNY Accessories, Catheter, G-U
GUIDEWIRE
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Sep 4, 1992 |
| Received | Mar 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921200
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.