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ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM

K980110 Class II Traditional
Decision Date
1998-04-10
Sponsor / Applicant
Endocare, Inc.

Technical Specification

510(k) Submission ID K980110
Product Code GEH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4350
Decision Date 1998-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM received FDA 510(k) clearance under submission number K980110, 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 1998-04-10.

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.