meddevicedb.com FDA Device Reference

SURGICAL SYSTEM WITH CRYOGUIDE

K002615 Class II Traditional
Decision Date
2000-11-13
Sponsor / Applicant
Endocare, Inc.

Technical Specification

510(k) Submission ID K002615
Product Code GEH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4350
Decision Date 2000-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL SYSTEM WITH CRYOGUIDE received FDA 510(k) clearance under submission number K002615, sponsored by Endocare, 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 2000-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.