Clearance Summary
PROD. NO. 01-132 - SUTURE REMOVAL KIT received FDA 510(k) clearance under submission number K964827, sponsored by Continental Medical Laboratories, 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 1997-02-14.
- Submission: K964827
- Applicant / Sponsor: Continental Medical Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1997-02-14
Classification & Regulation
This clearance is catalogued under FDA product code MCZ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.