CLINICAL GLASS THERMOMETER— 510(k) K942483

Name: FDA 510(k) clearance K942483
Creator: U.S. Food and Drug Administration
Published: 1995-03-28

Substantially Equivalent

Makol Medical Instruments Corp.

FDA 510(k) clearance K942483 for CLINICAL GLASS THERMOMETER, Substantially Equivalent on 1995-03-28. Applicant: Makol Medical Instruments Corp.. Device class: 2.

Clearance details

Applicant: Makol Medical Instruments Corp.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1994-05-25
Decision date: 1995-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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