510(k) K944232 ยท CAC Apparatus, Autotransfusion
AUTOFLO INTRA-OP SHED BLOOD AUTORTRANSFUSTION SYS
| Applicant | Haemonetics Corp., Braintree MA, US |
| Decision | Substantially Equivalent, Jul 20, 1995 |
| Received | Sep 1, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944232
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.