510(k) K883899 ยท BYI Percussor, Powered-Electric
MANUAL PERCUSSOR CUPS
| Applicant | Medical Components, Inc., Anoka MN, US |
| Decision | Substantially Equivalent, Dec 13, 1988 |
| Received | Sep 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883899
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.