ActiPatch— 510(k) K192234
Substantially EquivalentBioelectronics Corporation
FDA 510(k) clearance K192234 for ActiPatch, Substantially Equivalent on 2020-01-31. Applicant: Bioelectronics Corporation. Device class: 2.
Clearance details
- Applicant
- Bioelectronics Corporation
- Product code
- Code PQY
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Frederick, MD, US
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