Cleared Traditional

K864283 - SIMPLASTIN EXCEL

K864283 is an FDA 510(k) clearance for SIMPLASTIN EXCEL, 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 35-day FDA review.

K864283 · Organon Teknika Corp. · Hematology device
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Dec 1986
Decision
35d
Days
Class 2
Risk

K864283 is an FDA 510(k) clearance for the SIMPLASTIN EXCEL. Classified as Test, Time, Prothrombin (product code GJS), Class II - Special Controls.

Submitted by Organon Teknika Corp. (Kensington, US). The FDA issued a Cleared decision on December 4, 1986 after a review of 35 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 - K864283

510(k) Number K864283 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 30, 1986
Decision Date December 04, 1986
Days to Decision 35 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
78d faster than avg
Panel avg: 113d · This submission: 35d
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 K864283.
PROTHROMBIN TIME TEST
K872537 · Sclavo, Inc. · Aug 1987
THROMBOREL S
K872844 · Behring Diagnostics, Inc. · Aug 1987
PROTIME AUTOMATE TEST KIT
K864392 · American Bioproducts Co. · Jan 1987
THROMBOPLASTIN.FS
K864272 · American Dade · Nov 1986
THROMBOPLASTIN.C
K864273 · American Dade · Nov 1986
THROMBOPLASTIN.R
K864274 · American Dade · Nov 1986