AKUPORT M1— 510(k) K020567
Substantially EquivalentVibrant Health
FDA 510(k) clearance K020567 for AKUPORT M1, Substantially Equivalent on 2002-05-02. Applicant: Vibrant Health. Device class: 2.
Clearance details
- Applicant
- Vibrant Health
- Product code
- Code GZO
- Device class
- Class 2
- Regulation
- 21 CFR 882.1540
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beoeil, Quebec, CA
Recent devices under product code GZO
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