SAS Legionella Test, SAS Legionella Dipstick Test

FDA 510(k) K061496 · Sa Scientific , Ltd.

Substantially Equivalent

510(k) numberK061496

Submission

Device name
SAS Legionella Test, SAS Legionella Dipstick Test
Applicant
Sa Scientific , Ltd.
San Antonio, TX, US
Received
May 31, 2006
Decision date
June 28, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MJH – Legionella, Spp., Elisa
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3300
Specialty
Microbiology

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K113190Tru LegionellaMJH · Traditional Meridian Bioscience, Inc.02/24/2012SE
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K033051Legionella Pneumophila Igg/IgmMJH · Traditional Trinity Biotech USA11/26/2003SE
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K934965Binax Legionella Urinary Antigen EiaMJH · Traditional Binax, Inc.09/20/1994SE
K911356Legionella Stat Igg/Igm Test KitMJH · Traditional Whittaker Bioproducts, Inc.07/30/1992SE

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Questions and answers

When was SAS Legionella Test, SAS Legionella Dipstick Test cleared by the FDA?

SAS Legionella Test, SAS Legionella Dipstick Test (K061496) received a 510(k) decision of Substantially Equivalent on June 28, 2007, 393 days after the submission was received.

What is the product code of K061496?

The FDA product code is MJH – Legionella, Spp., Elisa, a Class II (moderate risk) device regulated under 21 CFR 866.3300.