Cleared Traditional

K802356 - VON WILLEBRAND FACTOR ASSAY

K802356 is the FDA 510(k) clearance for VON WILLEBRAND FACTOR ASSAY by Bio/Data Corp.. It is a Class 2 Hematology device (product code GGP) cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K802356 · Bio/Data Corp. · Hematology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1980
Decision
66d
Days
Class 2
Risk

K802356 is an FDA 510(k) clearance for the VON WILLEBRAND FACTOR ASSAY. Classified as Test, Qualitative And Quantitative Factor Deficiency (product code GGP), Class II - Special Controls.

Submitted by Bio/Data Corp. (Walker, US). The FDA issued a Cleared decision on December 1, 1980 after a review of 66 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 Bio/Data Corp. devices

Submission Details

510(k) Number K802356 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 26, 1980
Decision Date December 01, 1980
Days to Decision 66 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
47d faster than avg
Panel avg: 113d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 126
Devices cleared under the same product code (GGP) and FDA review panel - the closest regulatory comparables to K802356.
LANCER COAGENT HUMAN FACTOR 1X PLASMA
K812974 · Sherwood Medical Co. · Nov 1981
LANCER COAGENT HUMAN VACTOR VIII PLASMA
K812975 · Sherwood Medical Co. · Nov 1981
FACTOR VIII DEFICIENT PLASMA #B8D
K812431 · Sigma Chemical Co. · Sep 1981
HELENA FACTOR XII DEFICIENT
K792656 · Helena Laboratories · Jan 1980
HELENA FACTOR IX DEFICIENT SUBSTRATE
K792475 · Helena Laboratories · Dec 1979
HELENA FACTOR XI DEFICIENT SUBSTRATE
K792476 · Helena Laboratories · Dec 1979