Dako Elisa Rotavirus Kit- 96 Tests K440

FDA 510(k) K912666 · Dako Corp.

Substantially Equivalent

510(k) numberK912666

Submission

Device name
Dako Elisa Rotavirus Kit- 96 Tests K440
Applicant
Dako Corp.
Denmark, DK
Received
June 18, 1991
Decision date
February 14, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LIQ – Enzyme Linked Immunoabsorbent Assay, Rotavirus
Device class
Class I (low risk)
Regulation
21 CFR 866.3405
Specialty
Microbiology

Other 510(k)s with product code LIQ

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K990842SAS Rota TestLIQ · Traditional Sa Scientific, Inc.08/09/1999SE
K972895Vidas Rotavirus (RTV) AssayLIQ · Traditional Biomerieux Vitek, Inc.10/03/1997SE
K971585Immunocard Stat! RotavirusLIQ · Traditional Meridian Diagnostics, Inc.08/20/1997SE
K964424Rotavirus EiaLIQ · Traditional Trinity Biotech, Inc.08/08/1997SE
K965092Vidas Rotavirus AssayLIQ · Traditional Biomerieux Vitek, Inc.05/05/1997SE
K951208Rota-Dan Rapid Rotavirus Eia KitLIQ · Traditional Eldan Technologies, Ltd.02/14/1996SE
K942286Diarlex Rota-AdenoLIQ · Traditional Orion Diagnostica, Inc.12/14/1994SE
K933587Immunocard RotavirusLIQ · Traditional Meridian Diagnostics, Inc.02/03/1994SE
K932384Ideia(Tm) RotavirusLIQ · Traditional Dako Diagnostics , Ltd.12/27/1993SE
K915137Kallestad Rotavirus MicroplateLIQ · Traditional Bio-Rad Laboratories, Inc.03/04/1992SE

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Questions and answers

When was Dako Elisa Rotavirus Kit- 96 Tests K440 cleared by the FDA?

Dako Elisa Rotavirus Kit- 96 Tests K440 (K912666) received a 510(k) decision of Substantially Equivalent on February 14, 1992, 241 days after the submission was received.

What is the product code of K912666?

The FDA product code is LIQ – Enzyme Linked Immunoabsorbent Assay, Rotavirus, a Class I (low risk) device regulated under 21 CFR 866.3405.