Protein Base Ise Control

FDA 510(k) K880710 · Bionostics, Inc.

Substantially Equivalent

510(k) numberK880710

Submission

Device name
Protein Base Ise Control
Applicant
Bionostics, Inc.
Acton, MA, US
Received
February 22, 1988
Decision date
March 24, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJR – Electrolyte Controls (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

Other 510(k)s with product code JJR

510(k)DeviceApplicantDecision
K990971Easylyte Quality Control Kit, Models 2814, 2815, 2816JJR · Traditional Medica Corp.04/27/1999SE
K960592Electrolyte StandardsJJR · Traditional Phoenix Diagnostics, Inc.05/13/1996SE
K955630RNA Medical Hemat ControlJJR · Traditional Bionostics, Inc.03/01/1996SE
K951435Aalto Scientific Sweat Chloride Reference MaterialJJR · Traditional Aalto Scientific, Ltd.05/02/1995SE
K943925Sweat Controls for Cystic Fibrosis TestingJJR · Traditional Quantimetrix Corp.10/04/1994SE
K934641I-Stat Control Levels 1,2,3JJR · Traditional I-Stat Corp.12/09/1993SE
K912513Electrolyte ControlJJR · Traditional Verichem Laboratories, Inc.07/19/1991SE
K902266Electrolyte Controls (Assayed and Unassayed)JJR · Traditional Phoenix Diagnostics, Inc.06/06/1990SE
K894576Ciba Corning Certain LyteJJR · Traditional Ciba Corning Diagnostics Corp.10/30/1989SE
K895582Qclyte Protein-Based Ise ControlJJR · Traditional Baxter Healthcare Corp10/04/1989SE

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Questions and answers

When was Protein Base Ise Control cleared by the FDA?

Protein Base Ise Control (K880710) received a 510(k) decision of Substantially Equivalent on March 24, 1988, 31 days after the submission was received.

What is the product code of K880710?

The FDA product code is JJR – Electrolyte Controls (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.