510(k) K211342

Device
Sofia 2 Campylobacter FIA
Applicant
Quidel Corporation
510(k) number
K211342
Product code
LQP
Decision
Substantially Equivalent (SESE)
Decision date
2021-11-23
Date received
2021-05-03
Regulation
866.3110
Classification name
Campylobacter Spp.
Medical specialty
Microbiology
Review panel
Microbiology
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Michelle Bodien
Address
10165 Mckellar Ct. San Diego CA US 92121 92121

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LQP#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K210976Curian CampyMeridian Bioscience, Inc.2021-12-23
K191442Campylobacter ChekTechlab, Inc.2019-06-20
K191456Campylobacter Quik ChekTechlab, Inc.2019-06-20
K173217CAMPYLOBACTER QUIK CHEKTechlab, Inc.2018-01-22
K173219CAMPYLOBACTER CHEKTechlab, Inc.2018-01-22
K090700IMMUNOCARD STAT CAMPY, MODEL 751530Meridian Bioscience, Inc.2009-05-28
K083464PREMIER CAMPY, MODEL 618096Meridian Bioscience, Inc.2009-01-30
K982315PROSPECT CAMPYLOBACTER MICROPLATE ASSAYAlexon - Trend, Inc.1998-11-18
K880389MERITEC(TM)-CAMPY (JCL)Meridian Diagnostics, Inc.1988-04-12
K864027BBL CAMPYSLIDE(TM) TESTBd Becton Dickinson Vacutainer Systems Preanalytic1986-12-11
K862814COMPLEMENT-FIXATION TEST FOR CAMPYLOBACTER JEJUNIInstitute Virion , Ltd.1986-09-30