510(k) K901882 ยท KOQ Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
URESIL ENDOSCOPIC LASER OVERTUBE
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jul 27, 1990 |
| Received | Apr 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901882
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.