Clearance Summary
PARALLEL ACTION PLIERS received FDA 510(k) clearance under submission number K861953, sponsored by Med-Tool, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1986-06-06.
- Submission: K861953
- Applicant / Sponsor: Med-Tool, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1986-06-06
Classification & Regulation
This clearance is catalogued under FDA product code HTC and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.