RAPITEX(R) RF NEW— 510(k) K903852

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K903852 for RAPITEX(R) RF NEW, Substantially Equivalent on 1990-08-30. 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: 1990-08-21
Decision date: 1990-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerville, NJ, 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.