Clearance Summary
POST SURGICAL KIT/POST BIOPSY KIT received FDA 510(k) clearance under submission number K910011, sponsored by Dermatological Research Laboratories, 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 1991-03-27.
- Submission: K910011
- Applicant / Sponsor: Dermatological Research Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5075
- Decision date: 1991-03-27
Classification & Regulation
This clearance is catalogued under FDA product code MCY and 21 CFR 880.5075, within the General Hospital review panel as a Class II device.