510(k) K952833 ยท LYY Latex Patient Examination Glove
AMPRI
| Applicant | Ampri Rubberware Industries Sdn Bhd, Phase Ii 44300 Batang Kali, MY |
| Decision | Substantially Equivalent, Sep 5, 1995 |
| Received | Jun 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952833
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.