DSL Somatomedin-C (DSL #5600)

FDA 510(k) K875229 · Diagnostic Systems Laboratories, Inc.

Substantially Equivalent

510(k) numberK875229

Submission

Device name
DSL Somatomedin-C (DSL #5600)
Applicant
Diagnostic Systems Laboratories, Inc.
Webster, TX, US
Received
December 22, 1987
Decision date
July 1, 1988
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

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
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

More from Nichols Institute

510(k)DeviceDecision
K061758Active Renin IrmaCIB · Special 07/28/2006SE
K020945Axsym Intact PTH, Model 2G06CEW · Traditional 05/31/2002SE
K020128Active Free Beta-Hcg Elisa, Model DSL-10-8500JHI · Traditional 03/01/2002SE
K002128Active Inhibin-A Elisa, Model DSL-10-28100NDR · Traditional 12/05/2000SE
K001086Free Testosterone Enzyme Immunoassay, Model DSL-10-4900CDZ · Traditional 05/18/2000SE
K990138DSL Active Afp Elisa, Model DSL-10-8400LOJ · Traditional 06/21/1999SE
K981871C-Reactive Protein Elisa, Model Number DSL-10-42100DCK · Traditional 11/09/1998SE
K973244Active Psa Irma (DSL-9700)LTJ · Traditional 08/03/1998SE
K973243Active Psa Elisa (DSL-10-9700)LTJ · Traditional 08/03/1998SE
K981607Active Renin Irma Model Number DSL-25100CIB · Traditional 05/27/1998SE

Questions and answers

When was DSL Somatomedin-C (DSL #5600) cleared by the FDA?

DSL Somatomedin-C (DSL #5600) (K875229) received a 510(k) decision of Substantially Equivalent on July 1, 1988, 192 days after the submission was received.

What is the product code of K875229?

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