Cleared Traditional

K961550 - QUALITROL MONO CONTROL SERUM SET
(FDA 510(k) Clearance)

Sep 1996
Decision
155d
Days
Class 2
Risk

K961550 is an FDA 510(k) clearance for the QUALITROL MONO CONTROL SERUM SET. This device is classified as a System, Test, Infectious Mononucleosis (Class II - Special Controls, product code KTN).

Submitted by Consolidated Technologies, Inc. (Austin, US). The FDA issued a Cleared decision on September 24, 1996, 155 days after receiving the submission on April 22, 1996.

This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5640.

Submission Details

510(k) Number K961550 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 22, 1996
Decision Date September 24, 1996
Days to Decision 155 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement

Device Classification

Product Code KTN — System, Test, Infectious Mononucleosis
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5640

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