MONITEMP BLOOD PACK TEMP. MONITOR— 510(k) K800667

Name: FDA 510(k) clearance K800667
Creator: U.S. Food and Drug Administration
Published: 1980-04-16

Substantially Equivalent

Liquid Crystal Products, Inc.

FDA 510(k) clearance K800667 for MONITEMP BLOOD PACK TEMP. MONITOR, Substantially Equivalent on 1980-04-16. Applicant: Liquid Crystal Products, Inc.. Device class: 2.

Clearance details

Applicant: Liquid Crystal Products, Inc.
Product code: Code KSE
Device class: Class 2
Regulation: 21 CFR 864.9700
Advisory panel: Hematology
Date received: 1980-03-26
Decision date: 1980-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K802319 — HEMOTEMP TM1980-10-10

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