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TRANSDUCER PROTECTOR

K910821 Class II Traditional
Decision Date
1991-08-12
Sponsor / Applicant
Gelman Sciences, Inc.

Technical Specification

510(k) Submission ID K910821
Product Code FIB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1991-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSDUCER PROTECTOR received FDA 510(k) clearance under submission number K910821, sponsored by Gelman Sciences, 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 1991-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code FIB and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.