Clearance Summary
KIT, PREP SHAVE received FDA 510(k) clearance under submission number K760052, sponsored by M-C Ind., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1976-07-16.
- Submission: K760052
- Applicant / Sponsor: M-C Ind., Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1976-07-16
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.