Cleared Traditional

K933010 - BIOMERIEUX HEMOLAB COFAC VIII

K933010 is the FDA 510(k) clearance for BIOMERIEUX HEMOLAB COFAC VIII by Biomerieux Vitek, Inc.. It is a Class 2 Hematology device (product code GJT) cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K933010 · Biomerieux Vitek, Inc. · Hematology device
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Sep 1993
Decision
86d
Days
Class 2
Risk

K933010 is an FDA 510(k) clearance for the BIOMERIEUX HEMOLAB COFAC VIII. Classified as Plasma, Coagulation Factor Deficient (product code GJT), Class II - Special Controls.

Submitted by Biomerieux Vitek, Inc. (Hazelwood, US). The FDA issued a Cleared decision on September 15, 1993 after a review of 86 days - a notably fast clearance 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: 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 Biomerieux Vitek, Inc. devices

Submission Details

510(k) Number K933010 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 21, 1993
Decision Date September 15, 1993
Days to Decision 86 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 113d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GJT Plasma, Coagulation Factor Deficient
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 - GJT Plasma, Coagulation Factor Deficient

All 60
Devices cleared under the same product code (GJT) and FDA review panel - the closest regulatory comparables to K933010.
STAGO FACTOR VII-DEFICIENT PLASMA
K933440 · American Bioproducts Co. · Oct 1993
STAGO FACTOR X-DEFICIENT PLASMA
K933441 · American Bioproducts Co. · Oct 1993
STAGO FACTOR XI-DEFICIENT PLASMA
K933444 · American Bioproducts Co. · Oct 1993
CLOTTING FACTOR-11,-VII, -X DEFICIENT PLASMA
K924400 · Behring Diagnostics, Inc. · Jun 1993
CLOTTING FACTOR-VIII-IX-XI-XII DEFICIENT PLASMA
K924396 · Behring Diagnostics, Inc. · May 1993
CLOTTING FACTOR V DEFICIENT PLASMA
K924394 · Behring Diagnostics, Inc. · Dec 1992