Ap Reagent Cartridge

FDA 510(k) K861284 · Hi Chem, Inc.

Substantially Equivalent

510(k) numberK861284

Submission

Device name
Ap Reagent Cartridge
Applicant
Hi Chem, Inc.
Brea, CA, US
Received
April 7, 1986
Decision date
April 28, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CJE – Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1050
Specialty
Clinical Chemistry

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K941764Hichem Calcium Reagent for the Synchron CX3 Prod. No. 88808CJY · Traditional 05/13/1994SE
K902673Hi Chem Total Protein/Albumin Serum Range Lin STNDJJY · Traditional 07/17/1990SE
K863617Ion 2/4 Flow Cell Cleaner (Product #88656)JGS · Traditional 10/24/1986SE
K862027LDP Reagent Cartridge (No. 88216)CFJ · Traditional 06/13/1986SE
K861893GGT Reagent Cartridge (Product No. 88204)JXL · Traditional 06/05/1986SE
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K861419Hi Chem Diagnostics LDL Reagent CartridgeCFJ · Traditional 04/28/1986SE

Questions and answers

When was Ap Reagent Cartridge cleared by the FDA?

Ap Reagent Cartridge (K861284) received a 510(k) decision of Substantially Equivalent on April 28, 1986, 21 days after the submission was received.

What is the product code of K861284?

The FDA product code is CJE – Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1050.