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ActiPatch
BioElectronics Corporation · Model 088 · UDI-DI 00851329005050
10
510(k) clearances
9
Adverse events
1
Recalls
7
Facilities
Description
Back Pain Advanced long -Lasting Relief
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-09-29 | Regenesis Biomedical Inc | In the course of device testing, the firm determined that the affected devices may, under certain unusual clinical circumstance, be unable to generate a therapeutic dose of radio f |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.