510(k) K992652 ยท LIH Interferential Current Therapy
SD-730 IF-SDS, PERFECT PULSE IF-SDS
| Applicant | Skylark Device & Systems Co., Ltd., Taipei, TW |
| Decision | Substantially Equivalent, Feb 3, 2000 |
| Received | Aug 6, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992652
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.