Enzyme Immunoassay Anti-Sm/Rnp Antibody Test Kit

FDA 510(k) K940588 · Helix Diagnostics, Inc.

Substantially Equivalent

510(k) numberK940588

Submission

Device name
Enzyme Immunoassay Anti-Sm/Rnp Antibody Test Kit
Applicant
Helix Diagnostics, Inc.
West Sacramento, CA, US
Received
February 8, 1994
Decision date
April 20, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LKO – Anti-Rnp Antibody, Antigen And Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5100
Specialty
Immunology

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K993589Varelisa RNP AntibodiesLKO · Traditional Pharmacia & Upjohn Co.11/26/1999SE
K990624Autostat II Anti-Sm/Rnp ElisaLKO · Traditional Cogent Diagnotics , Ltd.04/28/1999SE
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K960091Enzyme Immunoassay Anti-Double Stranded DNA (Dsdna) Test KitLRM · Traditional 03/20/1996SE
K954723Enzyme Immunoassay Ana Screening Test KitLKJ · Traditional 12/15/1995SE
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K952253Enzyme Immunoassay Ena Plus Screening Test KitLLL · Traditional 08/24/1995SE
K951850Enzyme Immunoassay ANTI-JO-1 Antibody Test KitLJM · Traditional 07/18/1995SE
K951798Enzyme Immunoassay ANTI-SCI-70 Antibody Test KitLJM · Traditional 07/17/1995SE
K940510Enzyme Immunoassay Anti-Sm Antibody Test KitLKP · Traditional 04/20/1994SE

Questions and answers

When was Enzyme Immunoassay Anti-Sm/Rnp Antibody Test Kit cleared by the FDA?

Enzyme Immunoassay Anti-Sm/Rnp Antibody Test Kit (K940588) received a 510(k) decision of Substantially Equivalent on April 20, 1994, 71 days after the submission was received.

What is the product code of K940588?

The FDA product code is LKO – Anti-Rnp Antibody, Antigen And Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.