510(k) K182668 ยท IRP Massager, Powered Inflatable Tube
Rapid Reboot Compression Therapy System
| Applicant | Rapid Reboot Recovery Products, LLC, Lindon UT, US |
| Decision | Substantially Equivalent, Dec 14, 2018 |
| Received | Sep 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182668
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.