Cleared Traditional

K873757 - LABELING CHANGE COAT-A-COUNT MORPHINE I...

K873757 is the FDA 510(k) clearance for LABELING CHANGE COAT-A-COUNT MORPHINE I... by Diagnostic Products Corp.. It is a Class 2 Toxicology device (product code DJG) cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K873757 · Diagnostic Products Corp. · Toxicology device
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Oct 1987
Decision
41d
Days
Class 2
Risk

K873757 is an FDA 510(k) clearance for the LABELING CHANGE COAT-A-COUNT MORPHINE IN URINE. Classified as Enzyme Immunoassay, Opiates (product code DJG), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on October 15, 1987 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3650 - 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 Diagnostic Products Corp. devices

Submission Details

510(k) Number K873757 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 1987
Decision Date October 15, 1987
Days to Decision 41 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 87d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DJG Enzyme Immunoassay, Opiates
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3650
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 - DJG Enzyme Immunoassay, Opiates

All 126
Devices cleared under the same product code (DJG) and FDA review panel - the closest regulatory comparables to K873757.
REVISED LABELING FOR OPIATES
K874485 · Abbott Laboratories · Nov 1987
REVISED LABELING FOR MORPHINE TEST KIT
K874268 · Roche Diagnostic Systems, Inc. · Nov 1987
REVISED LABELING FOR SYVA OPIATE ASSAYS
K873898 · Syva Co. · Oct 1987
LABELING CHANGE COAT-A-COUNT SERUM MORPHINE
K873758 · Diagnostic Products Corp. · Oct 1987
ACA DU PONT URINE OPIATES (U OPI) SCREEN METHOD
K872391 · E.I. Dupont DE Nemours & Co., Inc. · Aug 1987
RESUBMISSION OF URINE HEROIN/MORPHINE KIT [I-125]
K871698 · Immunalysis Corporation · Jun 1987