CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST— 510(k) K910240

Name: FDA 510(k) clearance K910240
Creator: U.S. Food and Drug Administration
Published: 1991-02-26

Substantially Equivalent

Crystal Diagnostics, Inc.

FDA 510(k) clearance K910240 for CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST, Substantially Equivalent on 1991-02-26. Applicant: Crystal Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Crystal Diagnostics, Inc.
Product code: Code CHH
Device class: Class 1
Regulation: 21 CFR 862.1175
Advisory panel: Clinical Chemistry
Date received: 1991-01-22
Decision date: 1991-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woburn, MA, US

Download summary PDF View on FDA.gov ↗

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