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FDA 510(k)

OLYMPUS HYSTERORESECTOSCOPE

K-Number: K897003 · 1990-03-16

ApplicantOlympus Corp.
Decision Date1990-03-16
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OLYMPUS HYSTERORESECTOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1990-03-16 under 510(k) number K897003. 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 HYSTERORESECTOSCOPE?

OLYMPUS HYSTERORESECTOSCOPE is a medical device that received FDA 510(k) clearance on 1990-03-16. The listed applicant is Olympus Corp.. The 510(k) number is K897003.

When did OLYMPUS HYSTERORESECTOSCOPE receive FDA 510(k) clearance?

OLYMPUS HYSTERORESECTOSCOPE received FDA 510(k) clearance on 1990-03-16, under 510(k) number K897003.

Who is the listed applicant for OLYMPUS HYSTERORESECTOSCOPE?

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 HYSTERORESECTOSCOPE?

The FDA product code for OLYMPUS HYSTERORESECTOSCOPE is HIH.

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Other records listing Olympus Corp. as applicant

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K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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Related Devices (Code: HIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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