PATHROMTIN— 510(k) K932011

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K932011 for PATHROMTIN, Substantially Equivalent on 1993-10-25. Applicant: Behring Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code GFO
Device class: Class 2
Regulation: 21 CFR 864.7925
Advisory panel: Hematology
Date received: 1993-04-23
Decision date: 1993-10-25
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.