Clearance Summary
HAND HELD GONIOMETER received FDA 510(k) clearance under submission number K850082, sponsored by Chattanooga Group, 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 1985-04-04.
- Submission: K850082
- Applicant / Sponsor: Chattanooga Group, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.1520
- Decision date: 1985-04-04
Classification & Regulation
This clearance is catalogued under FDA product code KQW and 21 CFR 888.1520, within the Orthopedic review panel as a Class I device.