510(k) K130978 ยท PFW Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat
ZTX ULTRASONIC DIATHERMY DEVICE
| Applicant | Zetroz, Inc., Trumbull CT, US |
| Decision | Substantially Equivalent, Nov 6, 2013 |
| Received | Apr 9, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130978
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.