510(k) K052625 ยท NYN Stimulator, Electrical, Transcutaneous, For Arthritis
BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
| Applicant | Bionicare Medical Technologies, Inc., Sparks MD, US |
| Decision | Substantially Equivalent, Dec 5, 2005 |
| Received | Sep 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052625
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.