ActiPatch— 510(k) K192234
Substantially EquivalentBioelectronics Corporation
FDA 510(k) clearance K192234 for ActiPatch, Substantially Equivalent on 2020-01-31. Applicant: Bioelectronics Corporation.
Clearance details
- Applicant
- Bioelectronics Corporation
- Product code
- Code PQY
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Frederick, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.