510(k) K960802 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat
CUSHMAN MANUFACTURING, INC. ULTRA 6.0.
| Applicant | Cushman Mfg., Inc., Long Beach CA, US |
| Decision | Substantially Equivalent, Jun 18, 1996 |
| Received | Feb 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960802
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.