REDI-CHECK PHOTMETER Q.A.— 510(k) K923598

Name: FDA 510(k) clearance K923598
Creator: U.S. Food and Drug Administration
Published: 1992-10-14

Substantially Equivalent

Awareness Technology, Inc.

FDA 510(k) clearance K923598 for REDI-CHECK PHOTMETER Q.A., Substantially Equivalent on 1992-10-14. Applicant: Awareness Technology, Inc.. Device class: 2.

Clearance details

Applicant: Awareness Technology, Inc.
Product code: Code JFS
Device class: Class 2
Regulation: 21 CFR 862.1170
Advisory panel: Clinical Chemistry
Date received: 1992-07-20
Decision date: 1992-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm City, FL, US

Download summary PDF View on FDA.gov ↗

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