510(k) K902059 ยท CAC Apparatus, Autotransfusion
AUTOWAND(TM) 7XXX SERIES
| Applicant | Boehringer Laboratories, Norristown PA, US |
| Decision | Substantially Equivalent, Jul 24, 1990 |
| Received | May 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902059
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.