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AMS MALLEABLE OR JONAS SILICONE-SILVER

K792724 Class II Traditional
Decision Date
1980-09-09
Sponsor / Applicant
American Medical Systems, Inc.

Technical Specification

510(k) Submission ID K792724
Product Code FAE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.3630
Decision Date 1980-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMS MALLEABLE OR JONAS SILICONE-SILVER received FDA 510(k) clearance under submission number K792724, sponsored by American Medical Systems, 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 1980-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code FAE and 21 CFR 876.3630, within the Gastroenterology, Urology review panel as a Class II device.