Clearance Summary
GYMFORM ABS-A-ROUND received FDA 510(k) clearance under submission number K130074, sponsored by Well Brain International , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2013-08-15.
- Submission: K130074
- Applicant / Sponsor: Well Brain International , Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5850
- Decision date: 2013-08-15
Classification & Regulation
This clearance is catalogued under FDA product code NGX and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.