510(k) K893218 ยท CAC Apparatus, Autotransfusion
AP900/PRP MODULE AND ACCESSORIES, MODIFICATION
| Applicant | Electromedics, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jun 12, 1990 |
| Received | Apr 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893218
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.