510(k) K183169 ยท IRP Massager, Powered Inflatable Tube
Pulse 2.0, Pulse Pro 2.0
| Applicant | NormaTec Industries, LP, Watertown MA, US |
| Decision | Substantially Equivalent, Dec 27, 2018 |
| Received | Nov 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183169
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.