71110 DESK CHARGER

Exophthalmometer

WELCH ALLYN, INC.

The following data is part of a premarket notification filed by Welch Allyn, Inc. with the FDA for 71110 Desk Charger.

Pre-market Notification Details

• Device ID: K771900
• 510k Number: K771900
• Device Name: 71110 DESK CHARGER
• Classification: Exophthalmometer
• Applicant: WELCH ALLYN, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: HLS
• CFR Regulation Number: 886.1270 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1977-10-06
• Decision Date: 1977-11-09

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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