Cleared Traditional

K801668 - QUICK CEPT

K801668 is the FDA 510(k) clearance for QUICK CEPT by Laboratory Diagnostics Co., Inc.. It is a Class 2 Chemistry device (product code JHS) cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K801668 · Laboratory Diagnostics Co., Inc. · Chemistry device
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Aug 1980
Decision
23d
Days
Class 2
Risk

K801668 is an FDA 510(k) clearance for the QUICK CEPT. Classified as Differential Rate Kinetic Method, Cpk Or Isoenzymes (product code JHS), Class II - Special Controls.

Submitted by Laboratory Diagnostics Co., Inc. (Mchenry, US). The FDA issued a Cleared decision on August 13, 1980 after a review of 23 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 Laboratory Diagnostics Co., Inc. devices

Submission Details

510(k) Number K801668 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 21, 1980
Decision Date August 13, 1980
Days to Decision 23 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 88d · This submission: 23d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JHS Differential Rate Kinetic 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 - JHS Differential Rate Kinetic Method, Cpk Or Isoenzymes

All 24
Devices cleared under the same product code (JHS) and FDA review panel - the closest regulatory comparables to K801668.
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CPK(CK) IN VITRO DIAG. REAGENT SET
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CARDIOZYME PLUS CK-TOTAL #65046
K803169 · Harleco · Jan 1981
ESKACHEM, CK-MB REAGENT
K792023 · Smithkline Diagnostics, Inc. · Oct 1979
CK-NUC REAGENT
K790916 · Smithkline Diagnostics, Inc. · Jun 1979
SPIN CHEM CK-NAC REAGENT
K790917 · Smithkline Diagnostics, Inc. · Jun 1979