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FDA 510(k)

OLYMPUS OES LAPAROSCOPY SYSTEM

K-Number: K923982 · 1993-03-15

ApplicantOlympus Corp.
Decision Date1993-03-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS OES LAPAROSCOPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1993-03-15 under 510(k) number K923982. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS OES LAPAROSCOPY SYSTEM?

OLYMPUS OES LAPAROSCOPY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-15. The listed applicant is Olympus Corp.. The 510(k) number is K923982.

When did OLYMPUS OES LAPAROSCOPY SYSTEM receive FDA 510(k) clearance?

OLYMPUS OES LAPAROSCOPY SYSTEM received FDA 510(k) clearance on 1993-03-15, under 510(k) number K923982.

Who is the listed applicant for OLYMPUS OES LAPAROSCOPY SYSTEM?

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 OES LAPAROSCOPY SYSTEM?

The FDA product code for OLYMPUS OES LAPAROSCOPY SYSTEM is GCJ.

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Other records listing Olympus Corp. as applicant

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Related Devices (Code: GCJ)

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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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