BEHRING LASER NEPHELOMETER— 510(k) K761234

Name: FDA 510(k) clearance K761234
Creator: U.S. Food and Drug Administration
Published: 1990-06-07

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K761234 for BEHRING LASER NEPHELOMETER, Substantially Equivalent on 1990-06-07. Applicant: Behring Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code JZW
Device class: Class 1
Regulation: 21 CFR 866.4540
Advisory panel: Immunology
Date received: 1990-06-07
Decision date: 1990-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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