510(k) K160608 ยท IRP Massager, Powered Inflatable Tube
NormaTec Pulse and NormaTec Pulse Pro
| Applicant | NormaTec Industries, LP, Newton MA, US |
| Decision | Substantially Equivalent, Apr 13, 2016 |
| Received | Mar 3, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160608
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.