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FDA 510(k)

ENDOSCOPE AND ACCESSORIES

K-Number: K790071 · 1979-04-02

ApplicantOlympus Corp.
Decision Date1979-04-02
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1979-04-02 under 510(k) number K790071. The device is classified under product code GCP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPE AND ACCESSORIES?

ENDOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1979-04-02. The listed applicant is Olympus Corp.. The 510(k) number is K790071.

When did ENDOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

ENDOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1979-04-02, under 510(k) number K790071.

Who is the listed applicant for ENDOSCOPE AND ACCESSORIES?

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 ENDOSCOPE AND ACCESSORIES?

The FDA product code for ENDOSCOPE AND ACCESSORIES is GCP.

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Other records listing Olympus Corp. as applicant

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.

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: GCP)

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.

K954614EOS BRAND DISPOSABLE PROCTOSCOPENorth Eos Industries, Inc.K896505PORGES UNIVERSAL HANDLESPorges Corp.K896008MODEL 6500 MERCURY ARC LIGHT SOURCEMedical Dynamics, Inc.K862424STEERABLE CATHETER SYSTEMEndovationsK860103MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVEEndotherapeuticsK843683MODULAR FIBERSCOPE SYSTEMReichert Scientific Instruments

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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