FEVER LINE AND FEVER LINE PLUS— 510(k) K893803

Name: FDA 510(k) clearance K893803
Creator: U.S. Food and Drug Administration
Published: 1989-08-21

Substantially Equivalent

Liquid Crystal Sciences, Inc.

FDA 510(k) clearance K893803 for FEVER LINE AND FEVER LINE PLUS, Substantially Equivalent on 1989-08-21. Applicant: Liquid Crystal Sciences, Inc.. Device class: 2.

Clearance details

Applicant: Liquid Crystal Sciences, Inc.
Product code: Code KPD
Device class: Class 2
Regulation: 21 CFR 880.2200
Advisory panel: General Hospital
Date received: 1989-05-22
Decision date: 1989-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

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