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GRICE SOFT TISSUE BIOPSY KIT

K922161 Class II Traditional
Decision Date
1992-10-13
Sponsor / Applicant
Ideal Medical, Inc.

Technical Specification

510(k) Submission ID K922161
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1992-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRICE SOFT TISSUE BIOPSY KIT received FDA 510(k) clearance under submission number K922161, sponsored by Ideal Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1992-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.