Anti-Dsdna Kit, IM.77/771 (50/100 Test Kits)

FDA 510(k) K893036 · Amersham Corp.

Substantially Equivalent

510(k) numberK893036

Submission

Device name
Anti-Dsdna Kit, IM.77/771 (50/100 Test Kits)
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
April 24, 1989
Decision date
June 2, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LRM – Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5100
Specialty
Immunology

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K994424Diamedix Is-Anti-Dsdna Test SystemLRM · Traditional Diamedix Corp.02/18/2000SE
K993727Bindazyme Anti-Dsdna Eia KitLRM · Traditional The Binding Site, Ltd.12/21/1999SE
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K983422The Aptus (Automated) Applications of the DS DNA Elisa Test System Linked Immunosorbent…LRM · Traditional Zeus Scientific, Inc.11/18/1998SE

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Questions and answers

When was Anti-Dsdna Kit, IM.77/771 (50/100 Test Kits) cleared by the FDA?

Anti-Dsdna Kit, IM.77/771 (50/100 Test Kits) (K893036) received a 510(k) decision of Substantially Equivalent on June 2, 1989, 39 days after the submission was received.

What is the product code of K893036?

The FDA product code is LRM – Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.