Clearance Summary
ULTICARE 2500 TREATMENT CHAIR received FDA 510(k) clearance under submission number K791016, sponsored by American Health Care Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-06-27.
- Submission: K791016
- Applicant / Sponsor: American Health Care Industries, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6140
- Decision date: 1979-06-27
Classification & Regulation
This clearance is catalogued under FDA product code FRK and 21 CFR 880.6140, within the General Hospital review panel as a Class I device.