510(k) K852390 ยท KQX Goniometer, Ac-Powered
CMT 1000
| Applicant | Prestigeline, Inc., Brentwood NY, US |
| Decision | Substantially Equivalent, Jul 19, 1985 |
| Received | Jun 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852390
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.