LASER CERULOPLASMIN KIT(CERULOPLASMIN REAGENTS)— 510(k) K852247

Name: FDA 510(k) clearance K852247
Creator: U.S. Food and Drug Administration
Published: 1985-07-10

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K852247 for LASER CERULOPLASMIN KIT(CERULOPLASMIN REAGENTS), Substantially Equivalent on 1985-07-10. Applicant: Behring Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code DDB
Device class: Class 2
Regulation: 21 CFR 866.5210
Advisory panel: Immunology
Date received: 1985-05-23
Decision date: 1985-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: La Jolla, CA, US

Download summary PDF View on FDA.gov ↗

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