510(k) K221210 ยท PFW Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat
PainShield MD PLUS
| Applicant | Nanovibronix, Inc., Elmsford NY, US |
| Decision | Substantially Equivalent, Nov 23, 2022 |
| Received | Apr 27, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221210
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.