Cleared Traditional

CMV IGM ANTIBODY TEST (INDIRECT FLUORESCENT TEST)

K893465 · Immuno Concepts, Inc. · Microbiology
Jul 1989
Decision
83d
Days
Class 2
Risk

About This 510(k) Submission

K893465 is an FDA 510(k) clearance for the CMV IGM ANTIBODY TEST (INDIRECT FLUORESCENT TEST), a Antibody Igm,if, Cytomegalovirus Virus (Class II — Special Controls, product code LKQ), submitted by Immuno Concepts, Inc. (Sacramento, US). The FDA issued a Cleared decision on July 25, 1989, 83 days after receiving the submission on May 3, 1989. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.3175.

Submission Details

510(k) Number K893465 FDA.gov
FDA Decision Cleared SESE
Date Received May 03, 1989
Decision Date July 25, 1989
Days to Decision 83 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary —

Device Classification

Product Code LKQ — Antibody Igm,if, Cytomegalovirus Virus
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.3175

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