AMG MED BRAND CLINICAL GLASS THERMOMETER— 510(k) K940394

Name: FDA 510(k) clearance K940394
Creator: U.S. Food and Drug Administration
Published: 1994-05-04

Substantially Equivalent

Technolab Industries (Canada) , Ltd.

FDA 510(k) clearance K940394 for AMG MED BRAND CLINICAL GLASS THERMOMETER, Substantially Equivalent on 1994-05-04. Applicant: Technolab Industries (Canada) , Ltd.. Device class: 2.

Clearance details

Applicant: Technolab Industries (Canada) , Ltd.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1994-01-26
Decision date: 1994-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Quebec, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.