510(k) K922404 ยท KRI Accessory Equipment, Cardiopulmonary Bypass
TUBE GRIP
| Applicant | Georgia Medical Products, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Nov 23, 1992 |
| Received | May 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922404
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.