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FDA 510(k)

71110 DESK CHARGER

K-Number: K771900 · 1977-11-09

ApplicantWelch Allyn, Inc.
Decision Date1977-11-09
Product CodeHLS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

71110 DESK CHARGER 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 1977-11-09 under 510(k) number K771900. The device is classified under product code HLS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 71110 DESK CHARGER?

71110 DESK CHARGER is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K771900.

When did 71110 DESK CHARGER receive FDA 510(k) clearance?

71110 DESK CHARGER received FDA 510(k) clearance on 1977-11-09, under 510(k) number K771900.

Who is the listed applicant for 71110 DESK CHARGER?

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 71110 DESK CHARGER?

The FDA product code for 71110 DESK CHARGER is HLS.

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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