CLP GLYCOSYLATED HEMOGLOBIN CONTROL-NR— 510(k) K896335

Name: FDA 510(k) clearance K896335
Creator: U.S. Food and Drug Administration
Published: 1989-12-11

Substantially Equivalent

Creative Laboratory Products, Inc.

FDA 510(k) clearance K896335 for CLP GLYCOSYLATED HEMOGLOBIN CONTROL-NR, Substantially Equivalent on 1989-12-11. Applicant: Creative Laboratory Products, Inc.. Device class: 2.

Clearance details

Applicant: Creative Laboratory Products, Inc.
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 1989-11-03
Decision date: 1989-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, 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.