Cleared Traditional

K935058 - FACTOR

K935058 is an FDA 510(k) clearance for FACTOR, manufactured by Sigma Diagnostics, Inc.. The device is a Class 2 Hematology device with product code GJT cleared through the Traditional 510(k) pathway after a 137-day FDA review.

K935058 · Sigma Diagnostics, Inc. · Hematology device
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Mar 1994
Decision
137d
Days
Class 2
Risk

K935058 is an FDA 510(k) clearance for the FACTOR. Classified as Plasma, Coagulation Factor Deficient (product code GJT), Class II - Special Controls.

Submitted by Sigma Diagnostics, Inc. (St. Louis, US). The FDA issued a Cleared decision on March 7, 1994 after a review of 137 days - within the typical 510(k) review window.

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 Sigma Diagnostics, Inc. devices

FDA 510(k) Submission Details - K935058

510(k) Number K935058 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 21, 1993
Decision Date March 07, 1994
Days to Decision 137 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
24d slower than avg
Panel avg: 113d · This submission: 137d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GJT Device Classification - Class 2, Special Controls

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 74
Devices cleared under the same product code (GJT) and FDA review panel - the closest regulatory comparables to K935058.
FACTOR VIII DEFICIENT PLASMA
K935057 · Sigma Diagnostics, Inc. · Mar 1994
FACTOR X DEFICIENT PLASMA
K935054 · Sigma Diagnostics, Inc. · Mar 1994
FACTOR VII DEFICIENT PLASMA
K935056 · Sigma Diagnostics, Inc. · Mar 1994
STAGO FACTOR V-DEFICIENT PLASMA
K934605 · American Bioproducts Co. · Mar 1994
STAGO FACTOR II-DEFICIENT PLASMA
K934606 · American Bioproducts Co. · Mar 1994
STAGO FACTOR IX-DEFICIENT PLASMA
K933432 · American Bioproducts Co. · Nov 1993