Insulin-Like Growth Factor-I (Igf-I) Immunoradiometric Assay

FDA 510(k) K955390 · Corning Nichols Diagnostics

Substantially Equivalent

510(k) numberK955390

Submission

Device name
Insulin-Like Growth Factor-I (Igf-I) Immunoradiometric Assay
Applicant
Corning Nichols Diagnostics
San Juan Capistrano, CA, US
Received
November 24, 1995
Decision date
December 29, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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

510(k)DeviceApplicantDecision
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
K952505Insulin-Like Growth Factor I (Igf-I), Immunoradiometeric Assay (Irma)CFL · Traditional Nichols Institute07/03/1995SE
K946247IGFBP-3; Insulin-Like Growth Factor Binding PROTEIN-3CFL · Traditional Nichols Institute06/23/1995SE

Questions and answers

When was Insulin-Like Growth Factor-I (Igf-I) Immunoradiometric Assay cleared by the FDA?

Insulin-Like Growth Factor-I (Igf-I) Immunoradiometric Assay (K955390) received a 510(k) decision of Substantially Equivalent on December 29, 1995, 35 days after the submission was received.

What is the product code of K955390?

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