510(k) K780229 ยท KTD Orthosis, Abdominal
ABDOMINAL BELT
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 2, 1978 |
| Received | Feb 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780229
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.