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HD CAMERA HEAD OTV-S7PROH-HD-L08E

K083155 Class II Traditional
Decision Date
2009-01-13
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K083155
Product Code FET
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2009-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HD CAMERA HEAD OTV-S7PROH-HD-L08E received FDA 510(k) clearance under submission number K083155, sponsored by Olympus Medical Systems Corporation. 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 2009-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code FET and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.