TECHNICON RA SYSTEMS TOBRAMYCIN TEST METHOD— 510(k) K893913

Name: FDA 510(k) clearance K893913
Creator: U.S. Food and Drug Administration
Published: 1989-08-21

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K893913 for TECHNICON RA SYSTEMS TOBRAMYCIN TEST METHOD, Substantially Equivalent on 1989-08-21. Applicant: Technicon Instruments Corp.. Device class: 2.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code KLB
Device class: Class 2
Regulation: 21 CFR 862.3900
Advisory panel: Clinical Toxicology
Date received: 1989-05-30
Decision date: 1989-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

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