Clearance Summary
RAZOR, SCHICK DISPOSABLE received FDA 510(k) clearance under submission number K760342, sponsored by Parke-Davis Co.. 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 1976-08-11.
- Submission: K760342
- Applicant / Sponsor: Parke-Davis Co.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1976-08-11
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.