Cleared Traditional

K830672 - CREATINE KINASE REAGENT SET

K830672 is an FDA 510(k) clearance for CREATINE KINASE REAGENT SET, manufactured by Sterling Biochemical, Inc.. The device is a Class 2 Chemistry device with product code JHY cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K830672 · Sterling Biochemical, Inc. · Chemistry device
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Apr 1983
Decision
32d
Days
Class 2
Risk

K830672 is an FDA 510(k) clearance for the CREATINE KINASE REAGENT SET. Classified as Colorimetric Method, Cpk Or Isoenzymes (product code JHY), Class II - Special Controls.

Submitted by Sterling Biochemical, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 5, 1983 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1215 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sterling Biochemical, Inc. devices

FDA 510(k) Submission Details - K830672

510(k) Number K830672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 04, 1983
Decision Date April 05, 1983
Days to Decision 32 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 88d · This submission: 32d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JHY Device Classification - Class 2, Special Controls

Product Code JHY Colorimetric Method, Cpk Or Isoenzymes
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1215
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JHY Colorimetric Method, Cpk Or Isoenzymes

All 38
Devices cleared under the same product code (JHY) and FDA review panel - the closest regulatory comparables to K830672.
FLOW-PAC CPK REAGENT SET
K832977 · American Research Products Co. · Apr 1984
TANDEM - E-CKMB IMMUNOENZYMETRIC ASSAY
K832139 · Hybritech, Inc. · Aug 1983
WAKO CPK TEST
K832004 · Wako Chemicals USA, Inc. · Aug 1983
CREATINE KINASE-MB KIT
K820812 · Calbiochem-Behring Corp. · Apr 1982
REAGENT FOR DETERM. CREATINE PHOSPHOKINA
K800684 · Diagnostic Solutions, Inc. · May 1980
CPK ISOENZYME REAGENT
K791655 · Electrophoresis Corp. of America · Sep 1979