510(k) K965192 ยท BYI Percussor, Powered-Electric
THAIRAPY VEST SYSTEM
| Applicant | American Biosystems, Inc., St.Paul MN, US |
| Decision | Substantially Equivalent, Jun 24, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965192
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.