Cleared Traditional

K042941 - DADE BEHRING HEPARIN CALIBRATOR AND CON...

K042941 is the FDA 510(k) clearance for DADE BEHRING HEPARIN CALIBRATOR AND CON... by Dade Behring, Inc.. It is a Class 2 Hematology device (product code GIZ) cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K042941 · Dade Behring, Inc. · Hematology device
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Optimized for regulatory review, auditing and printing
Dec 2004
Decision
38d
Days
Class 2
Risk

K042941 is an FDA 510(k) clearance for the DADE BEHRING HEPARIN CALIBRATOR AND CONTROLS. Classified as Plasma, Control, Normal (product code GIZ), Class II - Special Controls.

Submitted by Dade Behring, Inc. (Newark, US). The FDA issued a Cleared decision on December 2, 2004 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.5425 - 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 Dade Behring, Inc. devices

Submission Details

510(k) Number K042941 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 2004
Decision Date December 02, 2004
Days to Decision 38 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
75d faster than avg
Panel avg: 113d · This submission: 38d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GIZ Plasma, Control, Normal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.5425
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 - GIZ Plasma, Control, Normal

All 9
Devices cleared under the same product code (GIZ) and FDA review panel - the closest regulatory comparables to K042941.
CONTROL PLASMA N
K023309 · Dade Behring, Inc. · Nov 2002
ACCUCLOT CONTROL I, MODEL A4089
K003328 · Sigma Diagnostics, Inc. · Mar 2001
CONTROL PLASMA N
K001256 · Dade Behring, Inc. · May 2000
ACCUCOLOR HIGH CALIBRATOR (A3089)
K973274 · Sigma Diagnostics, Inc. · Oct 1997
SPECIALTY ASSAYED CONTROL-1
K941737 · Helena Laboratories · Oct 1994
CONTROL PLASMA N
K924403 · Behring Diagnostics, Inc. · Feb 1994