Antinuclear Antibody (Ana) Positive Controls

FDA 510(k) K873249 · Cytotech, Inc.

Substantially Equivalent

510(k) numberK873249

Submission

Device name
Antinuclear Antibody (Ana) Positive Controls
Applicant
Cytotech, Inc.
San Diego, CA, US
Received
August 17, 1987
Decision date
September 22, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LKJ – Antinuclear Antibody, Antigen, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5100
Specialty
Immunology

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K024232Liquichek Anti-Ss-B Control, Positive, Catalog #113LKJ · Traditional Bio-Rad01/17/2003SE
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K863363Cytotech Toxoplasma Igg Enzyme ImmunoassayLGD · Traditional 11/13/1986SE
K862649Cytotech Cic Enzyme ImmunoassayDAK · Traditional 09/04/1986SE
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Questions and answers

When was Antinuclear Antibody (Ana) Positive Controls cleared by the FDA?

Antinuclear Antibody (Ana) Positive Controls (K873249) received a 510(k) decision of Substantially Equivalent on September 22, 1987, 36 days after the submission was received.

What is the product code of K873249?

The FDA product code is LKJ – Antinuclear Antibody, Antigen, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.