Ciba Corning Acs HCG Immunoassay

FDA 510(k) K904123 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK904123

Submission

Device name
Ciba Corning Acs HCG Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
September 6, 1990
Decision date
October 3, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHI – Visual, Pregnancy Hcg, Prescription Use
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1155
Specialty
Clinical Chemistry

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K172322Atellica IM Total hCG (ThCG)JHI · Traditional Siemens Healthcare Diagnostics, Inc.03/29/2018SE
K172257TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result…JHI · Traditional True Diagnostics, Inc.12/22/2017SE
K152768Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy…JHI · Traditional Assure Tech. Co., Ltd.02/24/2016SE
K130456Wunder Pregnancy TestJHI · Traditional James Nguyen04/08/2014SE
K132834Fastep S10 HCG Serum/Urine Combo TestJHI · Traditional Polymed Therapeutics, Inc.01/09/2014SE
K131166Sofia(R) HCG FiaJHI · Traditional Quidel Corp.08/02/2013SE
K123844Chemtrue HCG Pregnancy Urine Dipstick, HCG Pregnancy Urine Cassette Test, and HCG Combo…JHI · Traditional Chemtron Biotech, Inc.05/30/2013SE
K112101Fastep HCG Pregancy Serum/Urine Cassette and Dipstick TestsJHI · Traditional Polymed Therapeutics, Inc.07/17/2012SE

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K961657Ciba Corning 400 SystemCHL · Traditional 06/25/1996SE
K962021Ciba Corning 348 SystemCHL · Traditional 06/24/1996SE
K962126Acs CKMB II ImmunoassayJHS · Traditional 06/21/1996SE
K962041Acs LH2 ImmunoassayCEP · Traditional 06/21/1996SE
K961510Acs FRT4 ImmunoassayJJX · Traditional 06/17/1996SE
K960246Liquid Cardiac Marker 1,2,3 AssayedJJT · Traditional 04/23/1996SE
K955873Acs Phenytoin AssayLGR · Traditional 03/11/1996SE

Questions and answers

When was Ciba Corning Acs HCG Immunoassay cleared by the FDA?

Ciba Corning Acs HCG Immunoassay (K904123) received a 510(k) decision of Substantially Equivalent on October 3, 1990, 27 days after the submission was received.

What is the product code of K904123?

The FDA product code is JHI – Visual, Pregnancy Hcg, Prescription Use, a Class II (moderate risk) device regulated under 21 CFR 862.1155.