Cleared Traditional

K924892 - FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM (FDA 510(k) Clearance)

Class II Hematology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K924892 · Organon Teknika Corp. · Hematology device
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Apr 1994
Decision
569d
Days
Class 2
Risk

K924892 is an FDA 510(k) clearance for the FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM. Classified as Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control (product code DAT), Class II - Special Controls.

Submitted by Organon Teknika Corp. (Durham, US). The FDA issued a Cleared decision on April 21, 1994 after a review of 569 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7340 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Hematology submissions.

View all Organon Teknika Corp. devices

Submission Details

510(k) Number K924892 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 1992
Decision Date April 21, 1994
Days to Decision 569 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
456d slower than avg
Panel avg: 113d · This submission: 569d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DAT Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7340
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.