LASER RF CONTROL SERUM-QUALITY CONTROL SERUM— 510(k) K851537

Name: FDA 510(k) clearance K851537
Creator: U.S. Food and Drug Administration
Published: 1985-06-05

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K851537 for LASER RF CONTROL SERUM-QUALITY CONTROL SERUM, Substantially Equivalent on 1985-06-05. Applicant: Behring Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1985-04-16
Decision date: 1985-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: La Jolla, CA, US

Download summary PDF View on FDA.gov ↗

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