7 TRICYCLIC ANTIDE PRESSANTS— 510(k) K802245

Name: FDA 510(k) clearance K802245
Creator: U.S. Food and Drug Administration
Published: 1980-10-10

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K802245 for 7 TRICYCLIC ANTIDE PRESSANTS, Substantially Equivalent on 1980-10-10. Applicant: Technicon Instruments Corp.. Device class: 2.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code LFI
Device class: Class 2
Regulation: 21 CFR 862.3910
Advisory panel: Clinical Toxicology
Date received: 1980-09-16
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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