510(k) K973134 ยท LYY Latex Patient Examination Glove
OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED
| Applicant | Omnigrace , Ltd., Canton OH, US |
| Decision | Substantially Equivalent, Nov 6, 1997 |
| Received | Aug 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973134
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.