Clearance Summary
SENATEK received FDA 510(k) clearance under submission number K822993, sponsored by American Health Tech., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1982-10-26.
- Submission: K822993
- Applicant / Sponsor: American Health Tech., Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.5850
- Decision date: 1982-10-26
Classification & Regulation
This clearance is catalogued under FDA product code HST and 21 CFR 888.5850, within the Orthopedic review panel as a Class I device.