Androstenedione 125I Kit by Ria

FDA 510(k) K860559 · Immuchem Corp.

Substantially Equivalent

510(k) numberK860559

Submission

Device name
Androstenedione 125I Kit by Ria
Applicant
Immuchem Corp.
Carson, CA, US
Received
February 14, 1986
Decision date
March 14, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIZ – Radioimmunoassay, Androstenedione
Device class
Class I (low risk)
Regulation
21 CFR 862.1075
Specialty
Clinical Chemistry

Other 510(k)s with product code CIZ

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K963002Active Androstenedione EiaCIZ · Traditional Diagnostic Systems Laboratories, Inc.08/16/1996SE
K954755Coat-A-Count Direct AndrostenedioneCIZ · Traditional Diagnostic Products Corp.11/29/1995SE
K934751Active Androstanediol GlucuronideCIZ · Traditional Diagnostic Systems Laboratories, Inc.01/10/1994SE
K854673DSL Androstenedione Ria (DSL # 4200)CIZ · Traditional Diagnostic Systems Laboratories, Inc.01/22/1986SE
K854650DSL Active Androstenedione Ria (DSL #3800)CIZ · Traditional Diagnostic Systems Laboratories, Inc.12/13/1985SE
K844398Coat-A-Count Androstenedione Ria KitCIZ · Traditional Diagnostic Products Corp.12/10/1984SE
K842960Androstenedione by RiaCIZ · Traditional Radioassay Systems Laboratories, Inc.09/27/1984SE
K832452Androstenedione Test Set 125ICIZ · Traditional Wien Laboratories, Inc.09/12/1983SE
K801729Androstenedione Radioimmunoassay KitCIZ · Traditional Diagnostics Biochem Canada, Inc.10/31/1980SE

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K864144Luteinizing Hormone (Lh-Irma) Ria KitCEP · Traditional 11/24/1986SE
K854094Immuchem Covalent Coat a Solid Phase RadioimmunoasJLS · Traditional 02/28/1986SE
K830962Immuchem Covalent-Coat Ria KitDPO · Traditional 05/04/1983SE
K822509Covalent Coat Ria KitCFP · Traditional 09/28/1982SE
K822140Immuchem Covalent-CoatJKC · Traditional 08/05/1982SE
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Questions and answers

When was Androstenedione 125I Kit by Ria cleared by the FDA?

Androstenedione 125I Kit by Ria (K860559) received a 510(k) decision of Substantially Equivalent on March 14, 1986, 28 days after the submission was received.

What is the product code of K860559?

The FDA product code is CIZ – Radioimmunoassay, Androstenedione, a Class I (low risk) device regulated under 21 CFR 862.1075.