Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: GIZ FDA class 2

Plasma, Control, Normal

Hematology

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Plasma, Control, Normal (product code GIZ) is a quality control plasma preparation with normal coagulation activity, used to calibrate and monitor coagulation testing instruments and assays in hematology laboratories, ensuring test results fall within expected reference ranges. This device is classified as FDA Class 2, indicating moderate risk, and does not require premarket notification under the current classification. Regulated under 21 CFR 864.5425 in the Hematology specialty (HE), this device carries no special regulatory flags.

510(k) Clearances

20 matches
K Number
Device Name
STASIS - I, II AND III; SERATHAN - A, B; INTRIN - EA, SI CALCIUM CHLORIDE 0.02M; FIBRINOGEN CONTROL-NORMAL, LOW
DADE BEHRING HEPARIN CALIBRATOR AND CONTROLS
CONTROL PLASMA N
REFERENCE CHECK, CATALOG NUMBER-RCN-10
ACCUCLOT CONTROL I, MODEL A4089
CONTROL PLASMA N
COAGULATION CONTROL LEVEL 1 (NORMAL)
ACCUCOLOR HIGH CALIBRATOR (A3089)
THROMBOLYTIC ASSESSMENT SYSTEM PROTHROMBIN TIME TEST CONTROLS
SPECIALTY ASSAYED CONTROL-1
DVVTEST AND DVVCONFIRM LUPUS ANTICOAGULANT NORMAL AND ABNORMAL CONTROL PLASMA
CONTROL PLASMA N
COAGULATION REFERENCE PLASMA, NORMAL
UNICALIBRATOR KIT
COAGULATION REFERENCE PLASMA, NORMAL
NORMAL COAGULATION CONTROL PLASMA (NCCP)
ACS ANIMAL PLASMA COAGULATION CONTROL LEVEL I
ACS HUMAN PLASMA COAGULATION CONTROL LEVEL I
EDL NORMAL COAGULATION CONTROL
CLP NORMAL COAGULATION CONTROL

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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