Human Growth Hormone Enzyme Immunoassay MB-1015

FDA 510(k) K896643 · Medix Biotech, Inc.

Substantially Equivalent

510(k) numberK896643

Submission

Device name
Human Growth Hormone Enzyme Immunoassay MB-1015
Applicant
Medix Biotech, Inc.
Foster City, CA, US
Received
November 24, 1989
Decision date
December 29, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CFL – Radioimmunoassay, Human Growth Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1370
Specialty
Clinical Chemistry

Other 510(k)s with product code CFL

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K972761Sealite Sciences, Inc. Aqualite Human Growth Hormone AssayCFL · Traditional Sealite Sciences, Inc.09/25/1997SE
K971353DSL Active Non-Extraction Igf-I ElisaCFL · Traditional Diagnostic Systems Laboratories, Inc.05/12/1997SE
K970701DSL 1900 Active Human Growth Hormone Irma (DSL 1900)CFL · Traditional Diagnostic Systems Laboratories, Inc.04/02/1997SE
K962758DSL 9100 Igf-Ii IrmaCFL · Traditional Diagnostic Systems Laboratories, Inc.08/30/1996SE
K961678Human Growth Hormone Immunoassay KitCFL · Traditional Nichols Institute Diagnostics07/08/1996SE
K961172DSL Active Non-Extraction Igf-I IrmaCFL · Traditional Diagnostic Systems Laboratories, Inc.04/23/1996SE
K960551DSL Active Human Growth Hormone ElisaCFL · Traditional Diagnostic Systems Laboratories, Inc.03/06/1996SE
K955376Immulite HGHCFL · Traditional Diagnostic Products Corp.02/16/1996SE
K955390Insulin-Like Growth Factor-I (Igf-I) Immunoradiometric AssayCFL · Traditional Corning Nichols Diagnostics12/29/1995SE
K952505Insulin-Like Growth Factor I (Igf-I), Immunoradiometeric Assay (Irma)CFL · Traditional Nichols Institute07/03/1995SE

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Questions and answers

When was Human Growth Hormone Enzyme Immunoassay MB-1015 cleared by the FDA?

Human Growth Hormone Enzyme Immunoassay MB-1015 (K896643) received a 510(k) decision of Substantially Equivalent on December 29, 1989, 35 days after the submission was received.

What is the product code of K896643?

The FDA product code is CFL – Radioimmunoassay, Human Growth Hormone, a Class I (low risk) device regulated under 21 CFR 862.1370.