Cleared Traditional

K930235 - HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY

K930235 is an FDA 510(k) clearance for HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR ..., manufactured by Technidyne Corp.. The device is a Class 2 Hematology device with product code GGP cleared through the Traditional 510(k) pathway after a 240-day FDA review.

K930235 · Technidyne Corp. · Hematology device
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Sep 1993
Decision
240d
Days
Class 2
Risk

K930235 is an FDA 510(k) clearance for the HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY. Classified as Test, Qualitative And Quantitative Factor Deficiency (product code GGP), Class II - Special Controls.

Submitted by Technidyne Corp. (Edison, US). The FDA issued a Cleared decision on September 2, 1993 after a review of 240 days - an extended review cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7290 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Hematology review framework, consistent with the majority of Class II 510(k) submissions.

View all Technidyne Corp. devices

FDA 510(k) Submission Details - K930235

510(k) Number K930235 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 1993
Decision Date September 02, 1993
Days to Decision 240 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
127d slower than avg
Panel avg: 113d · This submission: 240d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GGP Device Classification - Class 2, Special Controls

Product Code GGP Test, Qualitative And Quantitative Factor Deficiency
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7290
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 - GGP Test, Qualitative And Quantitative Factor Deficiency

All 158
Devices cleared under the same product code (GGP) and FDA review panel - the closest regulatory comparables to K930235.
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IL TEST(TM) PROTEIN S
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K921449 · American Bioproducts Co. · Sep 1992