510(k) K972859 ยท BYI Percussor, Powered-Electric
FLUTTER D
| Applicant | Bradstreet Clinical Research Assoc., Inc., Brunswick NJ, US |
| Decision | Substantially Equivalent, Jun 5, 1998 |
| Received | Aug 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972859
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.