510(k) K960467 ยท LYY Latex Patient Examination Glove
POWDER FREE LATEX EXAMINATION GLOVE
| Applicant | Biopro, Inc., Chester NJ, US |
| Decision | Substantially Equivalent, May 24, 1996 |
| Received | Jan 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960467
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.