Calibrator Standard Kit for Astra System

FDA 510(k) K884227 · A-Kem, Inc.

Substantially Equivalent

510(k) numberK884227

Submission

Device name
Calibrator Standard Kit for Astra System
Applicant
A-Kem, Inc.
Clifton, NJ, US
Received
October 6, 1988
Decision date
December 9, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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More from Siemens Healthcare Diagnostics, Inc.

510(k)DeviceDecision
K884224Total Bilirubin Reagent Kit for Astra SystemsCIG · Traditional 12/15/1988SE
K884226Amylase Reagent Kit for Astra SystemsCJA · Traditional 12/09/1988SE
K884225Total Protein Reagent Kit for Astra SystemsCEK · Traditional 12/09/1988SE
K882587A-Kem Albumin Reagent Kit for Astra SystemCIX · Traditional 08/08/1988SE
K882586A-Kem Calcium Reagent Kit for Astra SystemCIC · Traditional 08/08/1988SE
K873132Bun Reagent KitLFP · Traditional 10/23/1987SE
K873131Creatinine Reagent KitCGX · Traditional 10/23/1987SE
K873130Wash Solution KitJJE · Traditional 10/23/1987SE
K873129Carbon Dioxide Reagent KitJFL · Traditional 10/23/1987SE
K873128Glucose Reagent KitCGA · Traditional 10/23/1987SE

Questions and answers

When was Calibrator Standard Kit for Astra System cleared by the FDA?

Calibrator Standard Kit for Astra System (K884227) received a 510(k) decision of Substantially Equivalent on December 9, 1988, 64 days after the submission was received.

What is the product code of K884227?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.