Cleared Traditional

K861879 - CK REAGENT CARTRIDGE (PRODUCT NO. 88213)
(FDA 510(k) Clearance)

May 1986
Decision
14d
Days
Class 2
Risk

K861879 is an FDA 510(k) clearance for the CK REAGENT CARTRIDGE (PRODUCT NO. 88213). This device is classified as a Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes (Class II - Special Controls, product code CGS).

Submitted by Hi Chem, Inc. (Brea, US). The FDA issued a Cleared decision on May 29, 1986, 14 days after receiving the submission on May 15, 1986.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1215.

Submission Details

510(k) Number K861879 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 1986
Decision Date May 29, 1986
Days to Decision 14 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CGS — Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1215

Similar Devices — CGS Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes

All 122
Pointe Scientific Creatinine Kinase (CK) Reagent Set
K191296 · Medtest DX · Aug 2020
SEKURE Creatine Kinase Assay
K182702 · Sekisui Diagnostics P.E.I., Inc. · Apr 2019
ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator
K160724 · Siemens Healthcare Diagnostics, Inc. · Sep 2016
RANDOX LIQUID CK-MB, RANDOX CK-MB CALIBRATOR
K123977 · Randox Laboratories, Ltd. · Nov 2013
CPK REAGENT
K112416 · Vital Diagnostics (Manufacturing) Ptyltd · Nov 2011
DIMENSION VISTA CREATINE KINASE FLEX REAGENT CARTRIDGE AND DIMENSION VISTA CREATINE KINASE MB FLEX REAGENT CARTRIDGE
K083465 · Siemens Healthcare Diagnostics · Feb 2009