510(k) K934782 ยท KRI Accessory Equipment, Cardiopulmonary Bypass
AMMEX TUBING ORGANIZER
| Applicant | Ammex Cardiopulmonary Corp., Houston TX, US |
| Decision | Substantially Equivalent, Nov 18, 1993 |
| Received | Oct 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934782
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.