SYNCHRON CX SYSTEMS PREALBUMIN CALIBRATOR

K994169 · Beckman Coulter, Inc. · JIS · Feb 3, 2000 · Clinical Chemistry

Device Facts

• Record ID: K994169
• Device Name: SYNCHRON CX SYSTEMS PREALBUMIN CALIBRATOR
• Applicant: Beckman Coulter, Inc.
• Product Code: JIS · Clinical Chemistry
• Decision Date: Feb 3, 2000
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 862.1150
• Device Class: Class 2

Intended Use

The SYNCHRON® CX Systems Prealbumin Calibrator is intended for use with the SYNCHRON CX Systems for the calibration of Prealbumin (PAB) reagent.

Device Story

SYNCHRON CX Systems Prealbumin Calibrator is a six-level, ready-to-use, human serum-based liquid calibrator set. It is used in clinical laboratory settings to establish reference points for the SYNCHRON CX Systems Prealbumin reagent. By calibrating the system, it enables accurate quantification of prealbumin levels in human patient specimens. The calibrator is processed from fresh frozen human plasma that has been defibrinated. It is designed for professional use by laboratory personnel to ensure the analytical accuracy of the prealbumin test system, which supports clinical assessment of patient nutritional status or inflammatory states.

Clinical Evidence

Bench testing only. Stability studies support a 24-month shelf-life claim. No clinical trials were required for this calibration device.

Technological Characteristics

Six-level liquid calibrator set; human serum-based; processed from defibrinated fresh frozen human plasma. Traceable to IFCC reference preparation CRM 470. Storage at +2°C to +8°C. No software or electronic components.

Indications for Use

Indicated for use on Beckman SYNCHRON CX Systems to calibrate prealbumin test systems for the measurement of prealbumin in human specimens.

Regulatory Classification

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

• Beckman Immunochemistry Systems CAL 3 (K854811)

Submission Summary (Full Text)

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Summary of Safety & Effectiveness SYNCHRON® CX Systems Prealbumin Calibrator

## 1.0 Submitted By:

Lucinda Stockert Staff Regulatory Specialist, Product Submissions Beckman Coulter, Inc. 200 S. Kraemer Blvd., W-104 Brea, California 92822-8000 Telephone: [phone] FAX: [phone]

# 2.0 Date Submitted:

December 6, 1999

# 3.0 Device Name(s):

# 3.1 Proprietary Names

SYNCHRON® CX Systems Prealbumin Calibrator

# 3.2 Classification Name

Calibrator, (21 CFR §862.1150)

# 4.0 Predicate Device(s):

| SYNCHRON Systems<br>Reagent | Predicate | Manufacturer | Docket<br>Number |
|-------------------------------------|---------------------------------------------|-----------------------|------------------|
| SYNCHRON® Systems<br>PAB Calibrator | Beckman<br>Immunochemistry<br>Systems CAL 3 | Beckman Coulter, Inc. | K854811 |

## 5.0 Description:

The SYNCHRON CX Systems Prealbumin Calibrator Set is a six level ready-to-use human serum-based liquid calibrator set manufactured by Beckman Coulter, Inc. Each kit contains 1 X 3 mL bottles of a specific level of calibrator (identified as Levels 1 to Level 6).

Mailing Address: 200 S. Kraemer Boulevard P.O. Box 8000 Brea, CA 92822-8000

Telephone: [phone] Facsimile: [phone] Internet: www.beckmancoulter.com

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Beckman Coulter, Inc., Section 510(k) Notification SYNCHRON® CX Systems Prealbumin Calibrator Summary of Safety & Effectiveness

### 5.0 Intended Use:

The SYNCHRON® CX Systems Prealbumin Calibrator is intended for use with the SYNCHRON CX Systems for the calibration of Prealbumin (PAB) reagent.

### 7.0 Comparison to Predicate(s):

| Reagent | Aspect/Characteristic | Comments |
|------------------------------------------|--------------------------------------------------------------------------------------------|--------------------------|
| SYNCHRON<br>Systems CX PAB<br>Calibrator | Source Material: Fresh frozen human<br>plasma that has been defibrinated and<br>processed. | Same as Beckman<br>CAL 3 |
| | Storage Temperature (+2°C to +8°C) | |
| | Liquid, ready-to-use form | |
| | Value Assignment Methodology | |
| | Traceable to the IFCC reference<br>preparation for plasma proteins, lot CRM<br>470. | |

| Reagent | Aspect/Characteristic | Comments |
|------------------------------------------|-----------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| SYNCHRON<br>Systems<br>PAB<br>Calibrator | Intended Use: | SYNCHRON CX Systems PAB Calibrator is<br>intended for use in calibration of SYNCHRON<br>CX Systems Prealbumin Reagent.<br>Beckman CAL 3 is intended for use in<br>calibration of albumin and prealbumin on<br>ARRAY®, ARRAY® 360, and IMMAGE™<br>Immunochemistry systems |
| | Levels of Analyte | SYNCHRON Systems PAB Calibrator: 6<br>levels<br>Beckman CAL 3: 1 level |

## 8.0 Summary of Performance Data:

The data in the Premarket Notification on safety and effectiveness supports a finding of substantial equivalence to products already in commercial distribution. Stress stability studies of the Prealbumin calibrator support the Beckman stability claim of 24 months.

This summary of safety and effectiveness is being submitted in accordance with the requirements of the Safe Medical Device Act of 1990 and the implementing regulation 21 CFR 807.92.

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3 2000 FEB

Food and Drug Administration 2098 Gaither Road Rockville MD 20850

Ms. Lucinda Stockert Staff Regulatory Specialist Beckman Coulter, Inc. 200 S. Kraemer Boulevard M/S W-104 Box 8000 Brea, California 92822-8000

Re: K994169

> Trade Name: SYNCHRON® CX Systems Prealbumin Calibrator Regulatory Class: II Product Code: JIS Dated: December 6, 1999 Received: December 10, 1999

Dear Ms. Stockert:

We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

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This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrh/dsma/dsmamain.html".

Sincerely yours,

Steven Butman

Steven I. Gutman, M.D., M.B.A. Director Division of Clinical Laboratory Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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page ⊥ of ⊥

510(k) Number (if known): Y 44 4 / 69

510(k) Number (If Known): n777169
Device Name: SYNCHRON® CX Systems

Prealbumin Calibrator

Indications for Use:

The SYNCHRON® CX Systems Prealbumin Calibrator, used in conjunction with SYNCHRON® Systems Prealbumin reagent, is intended for use on Beckman's SYNCHRON CX Systems for the calibration of prealbumin test systems.

Clinical Significance:

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.

Jean Cooper

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(Division Sign-Off)
Division of Clinical Laboratory Devices

Division of Clinical tory Devices 510(k) Number

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use (per 21 CFR 801.109)

OR

Over-the-Counter Use Optional Format 1-2-96