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FDA 510(k)

LX 150 LIGHT SOURCE

K-Number: K922095 · 1992-07-17

ApplicantWelch Allyn, Inc.
Decision Date1992-07-17
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LX 150 LIGHT SOURCE 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 1992-07-17 under 510(k) number K922095. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LX 150 LIGHT SOURCE?

LX 150 LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1992-07-17. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K922095.

When did LX 150 LIGHT SOURCE receive FDA 510(k) clearance?

LX 150 LIGHT SOURCE received FDA 510(k) clearance on 1992-07-17, under 510(k) number K922095.

Who is the listed applicant for LX 150 LIGHT SOURCE?

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 LX 150 LIGHT SOURCE?

The FDA product code for LX 150 LIGHT SOURCE is EQH.

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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: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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