510(k) K032840 ยท KOE Dilator, Urethral
ATRION MEDICAL QL INFLATION DEVICE
| Applicant | Atrion Medical Products, Inc., Arab AL, US |
| Decision | Substantially Equivalent, Mar 3, 2004 |
| Received | Sep 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032840
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.