510(k) K830150 ยท DWD Suction Control, Intracardiac, Cardiopulmonary Bypass
VEINPREP VEIN GRAFT PREP. KIT A277723
| Applicant | Atrium Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 28, 1983 |
| Received | Jan 17, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830150
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.