510(k) K820104 ยท KMT Tray, Fluoride, Disposable
NUPRO* GEL TRAY
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Feb 23, 1982 |
| Received | Jan 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820104
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.