Antithrombin III Assay

FDA 510(k) K781480 · Dade, Baxter Travenol Diagnostics, Inc.

Substantially Equivalent

510(k) numberK781480

Submission

Device name
Antithrombin III Assay
Applicant
Dade, Baxter Travenol Diagnostics, Inc.
Mchenry, IL, US
Received
August 28, 1978
Decision date
November 8, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JBQ – Antithrombin Iii Quantitation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7060
Specialty
Hematology

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K033775Hemosil Liquid Antithrombin XLJBQ · Special Instrumentation Laboratory CO01/02/2004SE
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Questions and answers

When was Antithrombin III Assay cleared by the FDA?

Antithrombin III Assay (K781480) received a 510(k) decision of Substantially Equivalent on November 8, 1978, 72 days after the submission was received.

What is the product code of K781480?

The FDA product code is JBQ – Antithrombin Iii Quantitation, a Class II (moderate risk) device regulated under 21 CFR 864.7060.