Elecsys Prolactin Assay

FDA 510(k) K964748 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK964748

Submission

Device name
Elecsys Prolactin Assay
Applicant
Boehringer Mannheim Corp.
Concord, CA, US
Received
November 26, 1996
Decision date
January 21, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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
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
K943811Enzyme-Linked Fluorescent ImmunoassayCFT · Traditional Biomerieux Vitek, Inc.11/02/1994SE

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Questions and answers

When was Elecsys Prolactin Assay cleared by the FDA?

Elecsys Prolactin Assay (K964748) received a 510(k) decision of Substantially Equivalent on January 21, 1997, 56 days after the submission was received.

What is the product code of K964748?

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