Cleared Traditional

K884702 - EASY-TEST PARTIAL THROMBOPLASTIN TIME P...

K884702 is the FDA 510(k) clearance for EASY-TEST PARTIAL THROMBOPLASTIN TIME P... by Em Diagnostic Systems, Inc.. It is a Class 2 Hematology device (product code GFO) cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K884702 · Em Diagnostic Systems, Inc. · Hematology device
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Jan 1989
Decision
79d
Days
Class 2
Risk

K884702 is an FDA 510(k) clearance for the EASY-TEST PARTIAL THROMBOPLASTIN TIME PTT #16629. Classified as Activated Partial Thromboplastin (product code GFO), Class II - Special Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on January 27, 1989 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7925 - the FDA hematology 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 Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K884702 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 1988
Decision Date January 27, 1989
Days to Decision 79 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
34d faster than avg
Panel avg: 113d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GFO Activated Partial Thromboplastin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7925
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 Hematology devices follow this clearance model.

Regulatory Peers - GFO Activated Partial Thromboplastin

All 36
Devices cleared under the same product code (GFO) and FDA review panel - the closest regulatory comparables to K884702.
APTT-EA REAGENT, AN ELLAGIC ACID ACTIVATED REAGENT
K900049 · Medical Diagnostic Technologies, Inc. · Jan 1990
ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT)
K896545 · Sigma Chemical Co. · Dec 1989
APTT-P REAGENT, A PARTICLE ACTIVATED REAGENT
K895255 · Medical Diagnostic Technologies, Inc. · Oct 1989
KD ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT
K884485 · King Diagnostics, Inc. · Dec 1988
UNIFAST ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST
K882325 · Sclavo, Inc. · Aug 1988
ALUMINA SILICA-ACTIVATED PARTIAL THROM
K820835 · Hyland Therapeutic Div., Travenol Laboratories · Apr 1982