Cleared Traditional

K882214 - SIMPLASTIN EXCEL S

K882214 is an FDA 510(k) clearance for SIMPLASTIN EXCEL S, manufactured by Organon Teknika Corp.. The device is a Class 2 Hematology device with product code GJS cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K882214 · Organon Teknika Corp. · Hematology device
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Jul 1988
Decision
36d
Days
Class 2
Risk

K882214 is an FDA 510(k) clearance for the SIMPLASTIN EXCEL S. Classified as Test, Time, Prothrombin (product code GJS), Class II - Special Controls.

Submitted by Organon Teknika Corp. (Durham, US). The FDA issued a Cleared decision on July 1, 1988 after a review of 36 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7750 - 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 Organon Teknika Corp. devices

FDA 510(k) Submission Details - K882214

510(k) Number K882214 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 1988
Decision Date July 01, 1988
Days to Decision 36 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
77d faster than avg
Panel avg: 113d · This submission: 36d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GJS Device Classification - Class 2, Special Controls

Product Code GJS Test, Time, Prothrombin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7750
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 - GJS Test, Time, Prothrombin

All 102
Devices cleared under the same product code (GJS) and FDA review panel - the closest regulatory comparables to K882214.
HELENA THROMBOPLASTIN REAGENT
K892050 · Helena Laboratories · Jun 1989
DADE THROMBOPLASTIN IS
K891169 · Baxter Healthcare Corp · Apr 1989
VISION(R) PROTHROMBIN TIME
K883441 · Abbott Laboratories · Sep 1988
CLP PROTHROMBIN TIME TEST
K880566 · Creative Laboratory Products, Inc. · Mar 1988
EASY-TEST PROTHROMBIN TIME PT ITEM NO. 16628
K875062 · Em Diagnostic Systems, Inc. · Feb 1988
THROMBOPLASTIN.C
K874592 · Baxter Healthcare Corp · Feb 1988