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ENDOSCOPE POSITION MARKING PROBE,ENDOSCOPE POSITION DETECTING UNIT

K134026 Class II Traditional
Decision Date
2014-03-07
Sponsor / Applicant
Olympus Medical Systems Corp.

Technical Specification

510(k) Submission ID K134026
Product Code PGU
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2014-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPE POSITION MARKING PROBE,ENDOSCOPE POSITION DETECTING UNIT received FDA 510(k) clearance under submission number K134026, sponsored by Olympus Medical Systems Corp.. 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 2014-03-07.

Classification & Regulation

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