TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT— 510(k) K900167

Name: FDA 510(k) clearance K900167
Creator: U.S. Food and Drug Administration
Published: 1990-01-22

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K900167 for TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT, Substantially Equivalent on 1990-01-22. Applicant: Behring Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code DCF
Device class: Class 2
Regulation: 21 CFR 866.5040
Advisory panel: Immunology
Date received: 1990-01-12
Decision date: 1990-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerville, NJ, US

Download summary PDF View on FDA.gov ↗

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