Clearance Summary
PINCH METER received FDA 510(k) clearance under submission number K812343, sponsored by Fred Sammons, 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 1981-09-11.
- Submission: K812343
- Applicant / Sponsor: Fred Sammons, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.1250
- Decision date: 1981-09-11
Classification & Regulation
This clearance is catalogued under FDA product code HRW and 21 CFR 888.1250, within the Orthopedic review panel as a Class I device.