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FDA 510(k)

WELCH ALLYN VIDEO OPHTHALMOSCOPE

K-Number: K951210 · 1995-06-06

ApplicantWelch Allyn, Inc.
Decision Date1995-06-06
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WELCH ALLYN VIDEO OPHTHALMOSCOPE 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 1995-06-06 under 510(k) number K951210. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELCH ALLYN VIDEO OPHTHALMOSCOPE?

WELCH ALLYN VIDEO OPHTHALMOSCOPE is a medical device that received FDA 510(k) clearance on 1995-06-06. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K951210.

When did WELCH ALLYN VIDEO OPHTHALMOSCOPE receive FDA 510(k) clearance?

WELCH ALLYN VIDEO OPHTHALMOSCOPE received FDA 510(k) clearance on 1995-06-06, under 510(k) number K951210.

Who is the listed applicant for WELCH ALLYN VIDEO OPHTHALMOSCOPE?

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 VIDEO OPHTHALMOSCOPE?

The FDA product code for WELCH ALLYN VIDEO OPHTHALMOSCOPE is HLI.

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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: HLI)

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.

K153080RTVue XR OCT Avanti with AngioVue SoftwareOptovue, Inc.K123316HEINE OMEGA 500Heine Optotechnik GmbH & Co. KGK121739IVUE WITH NORMATIVE DATABASEOptovue, Inc.K120057ENVISU SPECTRAL DOMAIN OPHTHALMIC IMAGING SYSTEM (SDOIS)Bioptigen, Inc.K120238RTVUE XR OCTOptovue, Inc.K111531RHA2020Annidis Health Systems Corp.

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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