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FDA 510(k)

WELCH ALLYN GLAUCOMA DETECTOR

K-Number: K941723 · 1994-06-06

ApplicantWelch Allyn, Inc.
Decision Date1994-06-06
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WELCH ALLYN GLAUCOMA DETECTOR 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 1994-06-06 under 510(k) number K941723. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELCH ALLYN GLAUCOMA DETECTOR?

WELCH ALLYN GLAUCOMA DETECTOR is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K941723.

When did WELCH ALLYN GLAUCOMA DETECTOR receive FDA 510(k) clearance?

WELCH ALLYN GLAUCOMA DETECTOR received FDA 510(k) clearance on 1994-06-06, under 510(k) number K941723.

Who is the listed applicant for WELCH ALLYN GLAUCOMA DETECTOR?

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 WELCH ALLYN GLAUCOMA DETECTOR?

The FDA product code for WELCH ALLYN GLAUCOMA DETECTOR is HOO.

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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: HOO)

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.

K930448MARCO PROJECTION PERIMETERMarco Ophthalmic, Inc.K873912RICHMOND VISUAL FIELD SCREENERRichmond Products, Inc.K864467HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREENKeeler Instruments, Inc.K860115DIGILAB CAMBRIDGE PERIMETERBio-RadK832800AUTOMATIC TANGENT SCREEN 50CooperVision, Inc.

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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