510(k) K053509 ยท MVV Device, Acupressure
ACUBAND ACUPRESSURE WRIST BAND DEVICE
| Applicant | Acuband, Inc., Little Silver NJ, US |
| Decision | Substantially Equivalent, Aug 16, 2006 |
| Received | Dec 16, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053509
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.