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AMS OPTILUME INFLATION SYRINGE

K900760 Class II Traditional
Decision Date
1990-05-17
Sponsor / Applicant
American Medical Systems, Inc.

Technical Specification

510(k) Submission ID K900760
Product Code KOE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5520
Decision Date 1990-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMS OPTILUME INFLATION SYRINGE received FDA 510(k) clearance under submission number K900760, 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 1990-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code KOE and 21 CFR 876.5520, within the Gastroenterology, Urology review panel as a Class II device.