510(k) K233480

Device
Access SHBG
Applicant
Beckman Coulter, Inc.
510(k) number
K233480
Product code
CDZ
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-08
Date received
2023-10-26
Regulation
862.1680
Classification name
Radioimmunoassay, Testosterones And Dihydrotestosterone
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Kate Oelberg
Address
1000 Lake Hazeltine Dr. Chaska MN US 55318 55318

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code CDZ#

510(k), Device, Applicant table
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K191350ACTIVE® Free Testosterone RIAImmunotech S.R.O.2019-12-20
K191533ADVIA Centaur Testosterone II (TSTII), ADVIA Centaur SHBGSiemens Healthcare Diagnostics, Inc.2019-08-28
K190121IDS SHBGImmunodiagnostic Systems , Ltd.2019-06-17
K182521FastPack IP Sex Hormone Binding Globulin ImmunoassayQualigen, Inc.2019-01-29
K181017Free Testosterone AccuBind ELISA Test SystemMonobind, Inc.2018-07-20
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K151529Dimension Vista LOCI Total Testosterone Flex reagent cartridge, Dimension Vista Testosterone CalibratorSiemens Healthcare Diagnostics, Inc.2016-02-11
K152185ARCHITECT SHBGBiokit, S.A.2016-02-11
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