510(k) K896821 ยท KOQ Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE
| Applicant | North American Sterilization & Packaging Co., Sparta NJ, US |
| Decision | Substantially Equivalent, Feb 9, 1990 |
| Received | Dec 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896821
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.