← Product Code [JIX](/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/JIX) · K063508

# DIMENSION VISTA PROTEIN 1 CALIBRATOR AND CONTROL L, M, H; PROTEIN 2 CALIBRATOR AND CONTROL L, H; PROTEIN 3 CALIBRATOR AN (K063508)

_Dade Behring, Inc. · JIX · Jan 23, 2007 · Clinical Chemistry · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/JIX/K063508

## Device Facts

- **Applicant:** Dade Behring, Inc.
- **Product Code:** [JIX](/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/JIX.md)
- **Decision Date:** Jan 23, 2007
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 862.1150
- **Device Class:** Class 2
- **Review Panel:** Clinical Chemistry

## Indications for Use

The Dimension Vista™ Protein 1 Calibrator is an in vitro diagnostic product for the calibration of the α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB) methods on the Dimension Vista® System. The Dimension Vista™ Protein 1 Control L, M, and H are for use as assayed intralaboratory quality controls for assessment of precision and analytical bias in the determination of α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB) methods on the Dimension Vista® System. The Dimension Vista™ Protein 2 Calibrator is an in vitro diagnostic product for the calibration of the antistreptolysin O (ASL), C-reactive protein (CRP), CardioPhase® high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF) methods on the Dimension Vista® System. The Dimension Vista™ Protein 2 Control L and H are for use as assayed intralaboratory quality controls for the assessment of precision and analytical bias in the determination of antistreptolysin O (ASL), C-reactive protein (CRP) and Rheumatoid Factor (RF) on the Dimension Vista® System. The Dimension Vista™ Protein 3 Calibrator is an in vitro diagnostic product for the calibration of the α1-microglobulin (A1MIC) and microalbumin (MALB) methods on the Dimension Vista® System. The Dimension Vista™ Protein 3 Control is for use as assayed intralaboratory quality controls for assessment of precision and analytical bias in the determination of α1-microglobulin (A1MIC) and microalbumin (MALB) on the Dimension Vista® System.

## Device Story

Dimension Vista™ Protein 1, 2, and 3 Calibrators and Controls are liquid or lyophilized human serum/urine-based products used to calibrate and monitor the performance of specific protein assays on the Dade Behring Dimension Vista® System. Calibrators establish the relationship between instrument signal and analyte concentration; controls serve as independent samples to verify assay precision and bias. These products are used in clinical laboratory settings by trained laboratory personnel. The healthcare provider uses the resulting quality control data to validate the accuracy of patient test results before reporting. The benefit is ensuring the reliability and consistency of diagnostic protein measurements, which supports accurate clinical decision-making.

## Clinical Evidence

No clinical data. Bench testing only. Stability studies conducted over 24 months at +2 to +8°C, including stress testing at +37°C and open-vial stability. Value assignment performed using reference curves across multiple runs, vials, and replicates on nephelometric instruments.

## Technological Characteristics

Multi-analyte products; Protein 1/2 are liquid human serum-based; Protein 3 is lyophilized polygeline-based with human source proteins. Designed for use on the Dimension Vista System. No specific materials or software algorithms described for the calibrators/controls themselves.

## Regulatory Identification

A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also § 862.2 in this part.)

## Special Controls

*Classification.* Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9.

## Predicate Devices

- Dimension Vista™ Protein 1 Calibrator (k062055)
- Dimension Vista™ Protein 1 Control L, M, H (k062055)
- Dimension Vista™ Protein 2 Calibrator (k062035)
- Dimension Vista™ Protein 2 Control L, H (k062035)
- Dimension Vista™ Protein 3 Calibrator (k061990)
- Dimension Vista™ Protein 3 Control (k061990)

## Submission Summary (Full Text)

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# 510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY

A. 510(k) Number:
k063508

B. Purpose for Submission:
510(k) premarket notification to manufacture and market the Dimension Vista™ Protein 1 Calibrator and the Dimension Vista™ Protein 1 Control (Low, Medium, and High). The calibrator and controls have been modified to include α1-acid glycoprotein (A1AG) and haptoglobin (HAPT).

510(k) premarket notification to manufacture and market the Dimension Vista™ Protein 2 Calibrator and the Dimension Vista™ Protein 2 Control (Low and High). The calibrator and controls have been modified to include antistreptolysin O (ASL).

510(k) premarket notification to manufacture and market the Dimension Vista™ Protein 3 Calibrator and the Dimension Vista™ Protein 3 Control. The calibrator and controls have been modified to include α₁-microglobulin (A1MIC).

C. Measurand:
None - submission is for clearance of calibrator and control material

D. Type of Test:
Calibrators and Controls

E. Applicant:
Dade Behring, Inc.

F. Proprietary and Established Names:
Dimension Vista™ Protein 1 Calibrator
Dimension Vista™ Protein 1 Control L
Dimension Vista™ Protein 1 Control M
Dimension Vista™ Protein 1 Control H
Dimension Vista™ Protein 2 Calibrator
Dimension Vista™ Protein 2 Control L
Dimension Vista™ Protein 2 Control H
Dimension Vista™ Protein 3 Calibrator
Dimension Vista™ Protein 3 Control

G. Regulatory Information:
1. Regulation section:
21 CFR § 862.1150 – Calibrator
21 CFR § 862.1660 – Quality control material (assayed and unassayed)
2. Classification:
Class II (calibrator)

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Class I, reserved (controls)

3. Product code:
JIX - Calibrator, multi-analyte mixture
JJY - Multi-analyte controls, all kinds (assayed and unassayed)

4. Panel:
Clinical Chemistry (75)

H. Intended Use:
1. Intended use(s):
See indications for use below.

2. Indication(s) for use:
The Dimension Vista™ Protein 1 Calibrator is an in vitro diagnostic product for the calibration of the α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB) methods on the Dimension Vista® System.

The Dimension Vista™ Protein 1 Control L, M, and H are for use as assayed intralaboratory quality controls for assessment of precision and analytical bias in the determination of α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB) methods on the Dimension Vista® System.

The Dimension Vista™ Protein 2 Calibrator is an in vitro diagnostic product for the calibration of the antistreptolysin O (ASL), C-reactive protein (CRP), CardioPhase® high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF) methods on the Dimension Vista® System.

The Dimension Vista™ Protein 2 Control L and H are for use as assayed intralaboratory quality controls for the assessment of precision and analytical bias in the determination of antistreptolysin O (ASL), C-reactive protein (CRP) and Rheumatoid Factor (RF) on the Dimension Vista® System.

The Dimension Vista™ Protein 3 Calibrator is an in vitro diagnostic product for the calibration of the α1-microglobulin (A1MIC) and microalbumin (MALB) methods on the Dimension Vista® System.

The Dimension Vista™ Protein 3 Control is for use as assayed intralaboratory quality controls for assessment of precision and analytical bias in the determination of α1-microglobulin (A1MIC) and microalbumin (MALB) on the Dimension Vista® System.

3. Special conditions for use statement(s):
For prescription use.

4. Special instrument requirements:

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For use with the Dade Behring Dimension Vista® System

## I. Device Description:

**Dimension Vista™ Protein 1 Calibrator**: Protein 1 Calibrator is a liquid, human serum based product containing α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB).

**Dimension Vista™ Protein 1 Controls L, M, and H**: Protein 1 Control L, M, and H are liquid, multi-analyte, human serum based products containing α1-acid glycoprotein (A1AG), C3 complement (C3), C4 complement (C4), haptoglobin (HAPT), Immunoglobulin A (IGA), Immunoglobulin G (IGG), Immunoglobulin M (IGM), and Prealbumin (PREALB) in three concentration ranges: low, medium, and high.

**Dimension Vista™ Protein 2 Calibrator**: Protein 2 Calibrator is a liquid, human serum based product containing antistreptolysin O (ASL), C-reactive protein (CRP), CardioPhase® high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF).

**Dimension Vista™ Protein 2 Controls L and H**: Protein 2 Control L and H are liquid, multi-analyte, human serum based products containing antistreptolysin O (ASL), C-reactive protein (CRP), high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF) in two concentrations: low and high.

**Dimension Vista™ Protein 3 Calibrator**: Protein 3 Calibrator is a lyophilized, polygeline, based product of human urinary and serum proteins containing α1-microglobulin (A1MIC) and microalbumin (MALB).

**Dimension Vista™ Protein 3 Control**: Protein 3 Control is a lyophilized, polygeline, and rabbit albumin based product containing urinary α1-microglobulin (A1MIC) and serum albumin of human origin.

Refer to the product labeling for assigned values for each constituent. All human materials were tested by FDA approved methods and found to be negative for the presence of antibodies to HIV-1, HIV-2, HBsAg, and HCV.

## J. Substantial Equivalence Information:

1. Predicate device name(s):

Dimension Vista™ Protein 1 Calibrator

Dimension Vista™ Protein 1 Control L

Dimension Vista™ Protein 1 Control M

Dimension Vista™ Protein 1 Control H

Dimension Vista™ Protein 2 Calibrator

Dimension Vista™ Protein 2 Control L

Dimension Vista™ Protein 2 Control H

Dimension Vista™ Protein 3 Calibrator

Dimension Vista™ Protein 3 Control

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2. Predicate 510(k) number(s):

k062055 - Dimension Vista™ Protein 1 Calibrator
k062055 - Dimension Vista™ Protein 1 Control L, M, H
k062035 - Dimension Vista™ Protein 2 Calibrator
k062035 - Dimension Vista™ Protein 2 Control L, H
k061990 - Dimension Vista™ Protein 3 Calibrator
k061990 - Dimension Vista™ Protein 3 Control

3. Comparison with predicates:

1. Dimension Vista™ Protein 1 Calibrator and Control (L, M, and H)

|  Similarities  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Form | Liquid, human serum | Liquid, human serum  |
|  Traceability to | ERM®-DA470 (CRM470) | ERM®-DA470 (CRM470)  |
|  Differences  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Constituents | C3 complement, C4 complement, IgA, IgG, IgM and prealbumin | C3 complement, C4 complement, IgA, IgG, IgM, prealbumin, α1-acid glycoprotein, and haptoglobin  |

2. Dimension Vista™ Protein 2 Calibrator and Control (L and H)

|  Similarities  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Form | Liquid, human serum | Liquid, human serum  |
|  Differences  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Traceability to | ERM®-DA470 (C470) and 1stBritish Standard 64/0023 | 1stInternational Standard, ERM®-DA470 (C470) and 1stBritish Standard 64/0023  |
|  Constituents | C-reactive protein (CRP), high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF) | antistreptolysin O (ASL), C-reactive protein (CRP), high sensitivity CRP (hsCRP), and Rheumatoid Factors (RF)  |

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3. Dimension Vista™ Protein 3 Calibrator and Control

|  Similarities  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Traceability to | ERM®-DA470 (C470) | ERM®-DA470 (C470)  |
|  Differences  |   |   |
| --- | --- | --- |
|  Item | Device | Predicate  |
|  Form | Lyophilized, polygeline, human based albumin | Lyophilized, polygeline, and rabbit albumin based product containing urinary and serum proteins of human origin  |
|  Constituents | C-reactive protein (CRP), high sensitivity CRP (hsCRP) and Rheumatoid Factors (RF) | antistreptolysin O (ASL), C-reactive protein (CRP), high sensitivity CRP (hsCRP), and Rheumatoid Factors (RF)  |

K. Standard/Guidance Document Referenced (if applicable):
Not Applicable

L. Test Principle:
Not Applicable

M. Performance Characteristics (if/when applicable): 3
1. Analytical performance:
a. Precision/Reproducibility:
Not Applicable
b. Linearity/assay reportable range:
Not Applicable
c. Traceability, Stability, Expected values (controls, calibrators, or methods):
Traceability
Protein 1 Calibrator, Protein 1 Control (L, M, and H), Protein 3 Calibrator, and Protein 3 Control are traceable to ERM®-DA470 (CRM470). Protein 2 Calibrator and Protein 2 Control (L and H) are traceable to 1st International Standard, ERM®-DA470 (C470) and 1st British Standard 64/0023.
Value Assignment
The calibrator master lot value is assigned vs. ERM®-DA470 (CRM470) and 1st International Standard. The commercial calibrator lot value is assigned with three reference curves, 4 runs, 3 vials, 4 replicates per vial tested on two nephelometric instruments for a total of 144 values. The control values are assigned using the procedure outlined for the calibrators. Values assigned to

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controls are calibrated by reference to protein standard preparations and are lot-dependent.

## Stability

The calibrators and the controls are tested per the same stability protocol. Products are stored at +2 to +8°C and the stability studies are conducted for 24 months using 3 vials and 3 replicates per vial. Testing cycles are 0, 12, 18 and 24 months. Additional stress testing is done at 6 months after storing at +37°C for two weeks. Once the products reach 50% shelf life stability, opened/punctured vial testing is performed on days 0, 4, 7, 9, 11, and 14.

d. Detection limit:
Not Applicable

e. Analytical specificity:
Not Applicable

f. Assay cut-off:
Not Applicable

2. Comparison studies:
a. Method comparison with predicate device:
Not Applicable
b. Matrix comparison:
Not Applicable

3. Clinical studies:
a. Clinical Sensitivity:
Not Applicable
b. Clinical specificity:
Not Applicable
c. Other clinical supportive data (when a. and b. are not applicable):
Not Applicable

4. Clinical cut-off:
Not Applicable

5. Expected values/Reference range:
Not Applicable

## N. Proposed Labeling:

The labeling is sufficient and it satisfies the requirements of 21 CFR Part 809.10.

## O. Conclusion:

The submitted information in this premarket notification is complete and supports a substantial equivalence decision.

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**Source:** [https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/JIX/K063508](https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/JIX/K063508)

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