510(k) K151834 ยท NGX Stimulator, Muscle, Powered, For Muscle Conditioning
BEMER Classic Set, BEMER Pro-Set
| Applicant | Bemer Int AG, Triesen, LI |
| Decision | Substantially Equivalent, Feb 22, 2017 |
| Received | Jul 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151834
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2021 | BEMER INT. AG Bemer-Set/ Pro-Set for the following models: REF. 410201 (BEMER Pro-Set), REF. 420201 (B.BOX Professional), REF. 420100 (B.BOX CLASSIC), REF. 410100 (BEMER Classic-Set), REF. 420200 (B.BOX Professio Terminated |
NGX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.