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FDA 510(k)

OES LAPARO-THORACO VIDEOSCOPE (RIGID)

K-Number: K955456 · 1996-02-22

ApplicantOlympus America, Inc.
Decision Date1996-02-22
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OES LAPARO-THORACO VIDEOSCOPE (RIGID) is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 1996-02-22 under 510(k) number K955456. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OES LAPARO-THORACO VIDEOSCOPE (RIGID)?

OES LAPARO-THORACO VIDEOSCOPE (RIGID) is a medical device that received FDA 510(k) clearance on 1996-02-22. The listed applicant is Olympus America, Inc.. The 510(k) number is K955456.

When did OES LAPARO-THORACO VIDEOSCOPE (RIGID) receive FDA 510(k) clearance?

OES LAPARO-THORACO VIDEOSCOPE (RIGID) received FDA 510(k) clearance on 1996-02-22, under 510(k) number K955456.

Who is the listed applicant for OES LAPARO-THORACO VIDEOSCOPE (RIGID)?

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

What is the FDA product code for OES LAPARO-THORACO VIDEOSCOPE (RIGID)?

The FDA product code for OES LAPARO-THORACO VIDEOSCOPE (RIGID) is HET.

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Other records listing Olympus America, Inc. as applicant

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Related Devices (Code: HET)

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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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