510(k) K954722 ยท EFB Handpiece, Air-Powered, Dental
MICRO-DISPENSER 7000 & MICRODISPENSER 8000
| Applicant | NOUVAG AG, Washington DC, US |
| Decision | Substantially Equivalent, Jan 16, 1996 |
| Received | Oct 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954722
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.