Prolactin (125) Radioimmunaoassay

FDA 510(k) K803273 · Corning Medical & Scientific

Substantially Equivalent

510(k) numberK803273

Submission

Device name
Prolactin (125) Radioimmunaoassay
Applicant
Corning Medical & Scientific
Mchenry, IL, US
Received
December 29, 1980
Decision date
January 16, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CFT – Radioimmunoassay, Prolactin (Lactogen)
Device class
Class I (low risk)
Regulation
21 CFR 862.1625
Specialty
Clinical Chemistry

Other 510(k)s with product code CFT

510(k)DeviceApplicantDecision
K971921Prolactin (PRL) Hormone Microplate ElisaCFT · Traditional Monobind06/24/1997SE
K970281Vitros Immunodiagnostic Products Prolactin Reagent Pack/CalibratorsCFT · Traditional Johnson & Johnson Clinical Diagnostics, Inc.02/25/1997SE
K970188Sealite Sciences, Inc. Aqualite ProlactinCFT · Traditional Sealite Sciences, Inc.02/20/1997SE
K964748Elecsys Prolactin AssayCFT · Traditional Boehringer Mannheim Corp.01/21/1997SE
K960561DSL Active Prolactin Elisa Model 10-4500CFT · Traditional Diagnostic Systems Laboratories, Inc.04/26/1996SE
K960060DSL Active Prolactin IrmaCFT · Traditional Diagnostic Systems Laboratories, Inc.02/29/1996SE
K954680Access Prolactin Assay (Modification)CFT · Traditional Bio-Rad Laboratories, Inc.10/20/1995SE
K953656Abbott Imx Prolactin(Modification)CFT · Traditional Abbott Mfg., Inc.10/03/1995SE
K953657Abbott Axsym Prolactin(Modification)CFT · Traditional Abbott Mfg., Inc.09/25/1995SE
K944698Auraflex Prolactin 200 Test Pack, Calibrator Pack, Dilvent 1CFT · Traditional Organon Teknika Corp.03/21/1995SE

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Questions and answers

When was Prolactin (125) Radioimmunaoassay cleared by the FDA?

Prolactin (125) Radioimmunaoassay (K803273) received a 510(k) decision of Substantially Equivalent on January 16, 1981, 18 days after the submission was received.

What is the product code of K803273?

The FDA product code is CFT – Radioimmunoassay, Prolactin (Lactogen), a Class I (low risk) device regulated under 21 CFR 862.1625.