DETERMINATION OF QUINIDINE— 510(k) K860049

Substantially Equivalent

Clinical Data, Inc.

FDA 510(k) clearance K860049 for DETERMINATION OF QUINIDINE, Substantially Equivalent on 1986-01-22. Applicant: Clinical Data, Inc.. Device class: 2.

Clearance details

Applicant: Clinical Data, Inc.
Product code: Code LBZ
Device class: Class 2
Regulation: 21 CFR 862.3320
Advisory panel: Clinical Toxicology
Date received: 1986-01-06
Decision date: 1986-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

Download summary PDF View on FDA.gov ↗

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