NEOTHROMITIN(R)— 510(k) K924395

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K924395 for NEOTHROMITIN(R), Substantially Equivalent on 1992-12-01. Applicant: Behring Diagnostics, Inc..

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code GPO
Advisory panel: Microbiology
Date received: 1992-08-31
Decision date: 1992-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerville, NJ, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.