Clearance Summary
CONPHAR PERCUSSION HAMMER(BUCK TYPE) received FDA 510(k) clearance under submission number K803174, sponsored by Conphar, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1980-12-30.
- Submission: K803174
- Applicant / Sponsor: Conphar, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.1700
- Decision date: 1980-12-30
Classification & Regulation
This clearance is catalogued under FDA product code GWZ and 21 CFR 882.1700, within the Neurology review panel as a Class I device.