510(k) K942823 ยท DWG Electrosurgical Device
MAHE INSTRUMENTS
| Applicant | Mahe Intl., Inc., Nashville TN, US |
| Decision | Substantially Equivalent, Dec 5, 1994 |
| Received | Jun 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942823
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.