510(k) K900731 ยท LWM Device, Electrical Dental Anesthesia
MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)
| Applicant | Medical Consultants Intl. , Ltd., Glen Rock NJ, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Feb 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900731
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.