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FDA 510(k)

CCD ENDOSCOPE AND ATTACHMENTS

K-Number: K801247 · 1980-07-28

ApplicantWelch Allyn, Inc.
Decision Date1980-07-28
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CCD ENDOSCOPE AND ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801247. 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 CCD ENDOSCOPE AND ATTACHMENTS?

CCD ENDOSCOPE AND ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K801247.

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

CCD ENDOSCOPE AND ATTACHMENTS received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801247.

Who is the listed applicant for CCD ENDOSCOPE AND ATTACHMENTS?

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

What is the FDA product code for CCD ENDOSCOPE AND ATTACHMENTS?

The FDA product code for CCD ENDOSCOPE AND ATTACHMENTS is GCP.

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Other records listing Welch Allyn, Inc. 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.

K243598Welch Allyn Connex® 360 (Multiple)K241411Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)K223381iExaminer System with Panoptic PlusK212473Welch Allyn Connex Central StationK191013Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry optionK181016Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System

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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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