Clearance Summary
I.M. SCALPEL HANDLE received FDA 510(k) clearance under submission number K810720, sponsored by Instrument Makar, 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 1981-04-03.
- Submission: K810720
- Applicant / Sponsor: Instrument Makar, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1981-04-03
Classification & Regulation
This clearance is catalogued under FDA product code GDZ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.