510(k) K904888 ยท CAC Apparatus, Autotransfusion
AUTOWAND(TM) 7XXX SERIES, MODIFICATION
| Applicant | Boehringer Laboratories, Norristown PA, US |
| Decision | Substantially Equivalent, Jan 16, 1991 |
| Received | Oct 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904888
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.