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FDA 510(k)

ILLIMINATOR, MODEL 265 NASAL

K-Number: K782142 · 1979-01-26

ApplicantWelch Allyn, Inc.
Decision Date1979-01-26
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ILLIMINATOR, MODEL 265 NASAL 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 1979-01-26 under 510(k) number K782142. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILLIMINATOR, MODEL 265 NASAL?

ILLIMINATOR, MODEL 265 NASAL is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K782142.

When did ILLIMINATOR, MODEL 265 NASAL receive FDA 510(k) clearance?

ILLIMINATOR, MODEL 265 NASAL received FDA 510(k) clearance on 1979-01-26, under 510(k) number K782142.

Who is the listed applicant for ILLIMINATOR, MODEL 265 NASAL?

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 ILLIMINATOR, MODEL 265 NASAL?

The FDA product code for ILLIMINATOR, MODEL 265 NASAL is ERA.

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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: ERA)

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.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, 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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