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OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE

K891451 Class II Traditional
Decision Date
1989-10-02
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K891451
Product Code HIH
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1690
Decision Date 1989-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE received FDA 510(k) clearance under submission number K891451, sponsored by Olympus Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1989-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code HIH and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.