510(k) K802279 ยท EWG Laser, Ent Microsurgical Carbon-Dioxide
VIDA 55 PULSE-ECHO ULTRASONIC DEVICE
| Applicant | Vida, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 15, 1980 |
| Received | Sep 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802279
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.