MERCURY AND GLASS FEVER THERMOMETER— 510(k) K911269

Name: FDA 510(k) clearance K911269
Creator: U.S. Food and Drug Administration
Published: 1991-05-15

Substantially Equivalent

Steridyne Corp.

FDA 510(k) clearance K911269 for MERCURY AND GLASS FEVER THERMOMETER, Substantially Equivalent on 1991-05-15. Applicant: Steridyne Corp.. Device class: 2.

Clearance details

Applicant: Steridyne Corp.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1991-03-22
Decision date: 1991-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riviera Beach, FL, US

Download summary PDF View on FDA.gov ↗

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