Immpulse Free Estriol Assay Reagents

FDA 510(k) K860900 · Sclavo, Inc.

Substantially Equivalent

510(k) numberK860900

Submission

Device name
Immpulse Free Estriol Assay Reagents
Applicant
Sclavo, Inc.
Sunnyvale, CA, US
Received
March 10, 1986
Decision date
April 28, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGI – Radioimmunoassay, Estriol
Device class
Class I (low risk)
Regulation
21 CFR 862.1265
Specialty
Clinical Chemistry

Other 510(k)s with product code CGI

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K974721Unconjugated Estriol Assay for the Bayer Immuno 1 System (in Vitro Diagnostic System)CGI · Traditional Bayer Corp.03/03/1998SE
K962875Active Ultrasensitive Unconjugated Estriol EiaCGI · Traditional Diagnostic Systems Laboratories, Inc.08/23/1996SE
K955356Active Ultra-Sensitive Unconjugated EstriolCGI · Traditional Diagnostic Systems Laboratories, Inc.05/15/1996SE
K932989Coat-A-Count Free EstriolCGI · Traditional Diagnostic Products Corp.12/19/1994SE
K944490Autodelfia Unconjugated Estriol (UE3) KitCGI · Traditional Wallac OY12/09/1994SE
K920576Amerlex-M High Sensitivity Unconjugated EstriolCGI · Traditional Eastman Kodak Company03/23/1992SE
K903359Microzyme Unconjugated Estriol Enzyme Immuno KitCGI · Traditional Immunotech Corp.08/22/1990SE
K850787Solid Phase Free Estriol Enzyme ImmunoassayCGI · Traditional Nms Pharmaceuticals, Inc.03/26/1985SE
K844767Radioimmunoassay of Human Serum Plasma or Urine toCGI · Traditional Biotecx Laboratories, Inc.02/01/1985SE
K844511TDX Total EstriolCGI · Traditional Abbott Laboratories01/18/1985SE

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Questions and answers

When was Immpulse Free Estriol Assay Reagents cleared by the FDA?

Immpulse Free Estriol Assay Reagents (K860900) received a 510(k) decision of Substantially Equivalent on April 28, 1986, 49 days after the submission was received.

What is the product code of K860900?

The FDA product code is CGI – Radioimmunoassay, Estriol, a Class I (low risk) device regulated under 21 CFR 862.1265.