Cleared Traditional

K924429 - OPUS CK-MB

K924429 is the FDA 510(k) clearance for OPUS CK-MB by Pb Diagnostic Systems, Inc.. It is a Class 2 Toxicology device (product code JHY) cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K924429 · Pb Diagnostic Systems, Inc. · Toxicology device
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Oct 1992
Decision
44d
Days
Class 2
Risk

K924429 is an FDA 510(k) clearance for the OPUS(R) CK-MB. Classified as Colorimetric Method, Cpk Or Isoenzymes (product code JHY), Class II - Special Controls.

Submitted by Pb Diagnostic Systems, Inc. (Westwood, US). The FDA issued a Cleared decision on October 15, 1992 after a review of 44 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.1215 - the FDA toxicology device 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 Pb Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K924429 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 01, 1992
Decision Date October 15, 1992
Days to Decision 44 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 87d · This submission: 44d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 Toxicology devices follow this clearance model.

Regulatory Peers - JHY Colorimetric Method, Cpk Or Isoenzymes

All 29
Devices cleared under the same product code (JHY) and FDA review panel - the closest regulatory comparables to K924429.
CK-MB METHOD FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO
K961412 · Bayer Corp. · Jun 1996
AURAFLEX CK-MB 200TEST PACK, CALIBRATOR PACK
K951638 · Organon Teknika Corp. · May 1995
IMX(R) STAT CK-MB
K931172 · Abbott Laboratories · Jun 1993
DU PONT ACA PLUS IMMUNOASSAY SYSTEM MB MCKMB METH.
K922700 · E.I. Dupont DE Nemours & Co., Inc. · Aug 1992
TANDEM ICON QSR CKMB IMMUNOENZYMETRIC ASSAY
K921763 · Hybritech, Inc. · Jun 1992
AMERLITE CK-MB ASSAY
K912766 · Amersham Corp. · Jul 1991