Coat-A-Count Insulin Kit

FDA 510(k) K821861 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK821861

Submission

Device name
Coat-A-Count Insulin Kit
Applicant
Diagnostic Products Corp.
Mchenry, IL, US
Received
June 24, 1982
Decision date
July 8, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CFP – Radioimmunoassay, Immunoreactive Insulin
Device class
Class I (low risk)
Regulation
21 CFR 862.1405
Specialty
Clinical Chemistry

Other 510(k)s with product code CFP

510(k)DeviceApplicantDecision
K963911Alpco/Mercodia Insulin ElisaCFP · Traditional American Laboratory Products Co., Ltd.11/01/1996SE
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K920109Imx InsulinCFP · Traditional Abbott Laboratories05/07/1992SE
K914820DSL Insulin Ria (DSL 1600)CFP · Traditional Diagnostic Systems Laboratories, Inc.01/09/1992SE
K903628Aia-Pack IriCFP · Traditional Tosoh Corp.09/07/1990SE
K901135Enzymun Test(R) InsulinCFP · Traditional Boehringer Mannheim Corp.04/03/1990SE
K896572Rep(Tm) Spe PLUS-30 ProceduresCFP · Traditional Helena Laboratories01/11/1990SE
K890837Ria-Gnost InsulinCFP · Traditional Cambridge Medical Technology04/26/1989SE
K851071Pharmacia Insulin RiaCFP · Traditional Pharmacia, Inc.04/12/1985SE
K841573Insulin Radioimmunoassay KitCFP · Traditional Sorin Biomedica, Fiat, USA, Inc.05/16/1984SE

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Questions and answers

When was Coat-A-Count Insulin Kit cleared by the FDA?

Coat-A-Count Insulin Kit (K821861) received a 510(k) decision of Substantially Equivalent on July 8, 1982, 14 days after the submission was received.

What is the product code of K821861?

The FDA product code is CFP – Radioimmunoassay, Immunoreactive Insulin, a Class I (low risk) device regulated under 21 CFR 862.1405.