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FDA 510(k)

FIBER OPTIC LARYNGOSCOPES W/BATTERY

K-Number: K830047 · 1983-01-18

ApplicantWelch Allyn, Inc.
Decision Date1983-01-18
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC LARYNGOSCOPES W/BATTERY 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 1983-01-18 under 510(k) number K830047. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC LARYNGOSCOPES W/BATTERY?

FIBER OPTIC LARYNGOSCOPES W/BATTERY is a medical device that received FDA 510(k) clearance on 1983-01-18. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K830047.

When did FIBER OPTIC LARYNGOSCOPES W/BATTERY receive FDA 510(k) clearance?

FIBER OPTIC LARYNGOSCOPES W/BATTERY received FDA 510(k) clearance on 1983-01-18, under 510(k) number K830047.

Who is the listed applicant for FIBER OPTIC LARYNGOSCOPES W/BATTERY?

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 FIBER OPTIC LARYNGOSCOPES W/BATTERY?

The FDA product code for FIBER OPTIC LARYNGOSCOPES W/BATTERY is CCW.

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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: CCW)

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.

K191602APA Oxy BladeVenner Medical (Singapore) Pte, Ltd.K163412Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)Girgis Scope, LLCK121378AIRTRAQ SP AIRTRAQ AVANTProdol Meditec , Ltd.K063477NOVAMED MRI CONDITIONAL LARYNGOSCOPE SETNovamed, LLCK062523TRU-MR LARYNGOSCOPE SETTruphatek International, Ltd.K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002Minrad, 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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