ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set

FDA 510(k) K143075 · Tosoh Bioscience, Inc.

Substantially Equivalent

510(k) numberK143075

Submission

Device name
ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set
Applicant
Tosoh Bioscience, Inc.
South San Franciso, CA, US
Received
October 27, 2014
Decision date
July 2, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CDZ – Radioimmunoassay, Testosterones And Dihydrotestosterone
Device class
Class I (low risk)
Regulation
21 CFR 862.1680
Specialty
Clinical Chemistry

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Questions and answers

When was ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set cleared by the FDA?

ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set (K143075) received a 510(k) decision of Substantially Equivalent on July 2, 2015, 248 days after the submission was received.

What is the product code of K143075?

The FDA product code is CDZ – Radioimmunoassay, Testosterones And Dihydrotestosterone, a Class I (low risk) device regulated under 21 CFR 862.1680.