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FDA 510(k)

OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE

K-Number: K891451 · 1989-10-02

ApplicantOlympus Corp.
Decision Date1989-10-02
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1989-10-02 under 510(k) number K891451. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE?

OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE is a medical device that received FDA 510(k) clearance on 1989-10-02. The listed applicant is Olympus Corp.. The 510(k) number is K891451.

When did OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE receive FDA 510(k) clearance?

OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE received FDA 510(k) clearance on 1989-10-02, under 510(k) number K891451.

Who is the listed applicant for OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE?

The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE?

The FDA product code for OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE is HIH.

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Other records listing Olympus Corp. as applicant

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Related Devices (Code: HIH)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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