510(k) K030332 ยท NYN Stimulator, Electrical, Transcutaneous, For Arthritis
MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
| Applicant | Bionicare Medical Technologies, Inc., Sparks MD, US |
| Decision | Substantially Equivalent, Jun 6, 2003 |
| Received | Jan 31, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030332
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.