TECHNICON RA-PHENOBARBITAL— 510(k) K884419

Name: FDA 510(k) clearance K884419
Creator: U.S. Food and Drug Administration
Published: 1988-11-22

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K884419 for TECHNICON RA-PHENOBARBITAL, Substantially Equivalent on 1988-11-22. Applicant: Technicon Instruments Corp.. Device class: 2.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code DLZ
Device class: Class 2
Regulation: 21 CFR 862.3660
Advisory panel: Clinical Toxicology
Date received: 1988-10-20
Decision date: 1988-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

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