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.. Device class: 1.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code GPO
Device class: Class 1
Regulation: 21 CFR 866.3500
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 ↗

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