Cleared Traditional

K870106 - COAT-A-COUNT IRMA HCG KIT AND ITS COMPONENTS

K870106 is an FDA 510(k) clearance for COAT-A-COUNT IRMA HCG KIT AND ITS COMPO..., manufactured by Diagnostic Products Corp.. The device is a Class 2 Chemistry device with product code JHI cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K870106 · Diagnostic Products Corp. · Chemistry device
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Mar 1987
Decision
60d
Days
Class 2
Risk

K870106 is an FDA 510(k) clearance for the COAT-A-COUNT IRMA HCG KIT AND ITS COMPONENTS. Classified as Visual, Pregnancy Hcg, Prescription Use (product code JHI), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on March 13, 1987 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1155 - 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 Diagnostic Products Corp. devices

FDA 510(k) Submission Details - K870106

510(k) Number K870106 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 12, 1987
Decision Date March 13, 1987
Days to Decision 60 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
28d faster than avg
Panel avg: 88d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JHI Device Classification - Class 2, Special Controls

Product Code JHI Visual, Pregnancy Hcg, Prescription Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1155
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 - JHI Visual, Pregnancy Hcg, Prescription Use

All 282
Devices cleared under the same product code (JHI) and FDA review panel - the closest regulatory comparables to K870106.
TANDEM(R) M-PAK(TM) TOTAL B-HCG IMMUNOENZY. ASSAY
K870521 · Hybritech, Inc. · Apr 1987
ACA HUMAN CHORIONIC GONADOTROPIN (HCG) METHOD
K870672 · E.I. Dupont DE Nemours & Co., Inc. · Apr 1987
UBIMAGIWEL(TM)HCG QUANTITATIVE AND QUALITATIVE
K864174 · United Biotech, Inc. · Mar 1987
TANDEMR ICONR II HCG(SERUM) IMMUNOENZYMETRIC ASSAY
K865057 · Hybritech, Inc. · Mar 1987
VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044
K870259 · Leeco Diagnostics, Inc. · Mar 1987
SYNTRON BIORESEARCH MICROCHECK HCG PREGNANCY TEST
K865076 · Syntron Bioresearch, Inc. · Feb 1987