LIQUICHEK ANTI-SMOOTH MUSCLE CONTROL, POSITIVE, CATALOG #129

K024224 · Bio-Rad · DHN · Jan 15, 2003 · Immunology

Device Facts

• Record ID: K024224
• Device Name: LIQUICHEK ANTI-SMOOTH MUSCLE CONTROL, POSITIVE, CATALOG #129
• Applicant: Bio-Rad
• Product Code: DHN · Immunology
• Decision Date: Jan 15, 2003
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 866.5100
• Device Class: Class 2

Intended Use

The new Liquichek™ Anti-Smooth Muscle Control, Positive, is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing for the detection of smooth muscle autoantibodies.

Device Story

Liquichek™ Anti-Smooth Muscle Control, Positive is a liquid, human serum-based quality control material. It is used in clinical laboratories to monitor the performance and accuracy of indirect immunofluorescent (IIF) testing procedures for detecting smooth muscle autoantibodies. The control is provided in a ready-to-use liquid form and stored at 2°C to 8°C. Laboratory personnel use the control alongside patient samples during routine testing. By comparing the observed results of the control against expected performance ranges, clinicians and laboratory technicians verify the validity of the assay run. This process ensures the reliability of patient test results, aiding in the accurate diagnosis and management of autoimmune conditions associated with smooth muscle autoantibodies.

Clinical Evidence

No clinical data. Bench testing only.

Technological Characteristics

Human serum-based control material with added preservatives. Liquid form. Storage at 2°C to 8°C. Designed for use in indirect immunofluorescent (IIF) assays.

Indications for Use

Indicated for use as an unassayed quality control material to monitor the performance of indirect immunofluorescent assays designed to detect smooth muscle autoantibodies in human serum samples.

Regulatory Classification

Identification

An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjögren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).

Predicate Devices

• Kallestad™ Autoantibody Positive Control (K792610)

Submission Summary (Full Text)

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K024224

## Summarv of Safety and Effectiveness Liquichek™ Anti-Smooth Muscle Control, Positive

#### 1.0 Submitter

JAN 1 5 2003

Bio-Rad Laboratories 9500 Jeronimo Road, Irvine, California 92618-2017 [phone] Telephone: [phone] Fax:

# Contact Person

Yvette Lloyd Senior Regulatory Affairs Specialist Telephone: [phone]

# Date of Summary Preparation

December 20, 2002

#### 2.0 Device Identification

| Product Trade Name: | Liquichek™ ANA Control Speckled Pattern, Positive |
|---------------------|-----------------------------------------------------------------------|
| Common Name: | Antinuclear Antibody, Indirect Immunofluorescent,<br>Antigen, Control |
| Classifications: | Class II |
| Product Code: | 82DBE |
| Regulation Number: | 21 CFR 866.5100 |

#### 3.0 Device to Which Substantial Equivalence is Claimed

Kallestad ™ Autoantibody Positive Control Bio-Rad Laboratories

510 (k) Number: K792610

#### 4.0 Description of Device

This product is prepared from human serum with added preservatives. The control is provided in liquid form for convenience.

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#### Statement of Intended Use 5.0

The new Liquichek™ Anti-Smooth Muscle Control, Positive, is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing for the detection of smooth muscle autoantibodies.

#### Comparison of the new device with the Predicate Device 6.0

This control is substantially equivalent to the following quality control material for autoimmune analysis that is currently in the market:

Kallestad™ Autoantibody Positive Control Bio-Rad Laboratories

510 (k) Number: K792610

Table 1. Similarities and Differences between new and predicate device.

| Characteristics | Liquichek™ Anti-Smooth Muscle<br>Control, Positive<br>(New Device) | Kallestad™ Autoantibody Positive<br>Control<br>(Predicate Device) |
|-----------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Similarities | | |
| Intended Use | The Liquichek™ Anti-Smooth<br>Muscle Control, Positive, is<br>intended for use as an unassayed<br>quality control to monitor indirect<br>immunofluorescent testing for the<br>detection of smooth muscle<br>autoantibodies. | The Autoantibody Positive Control<br>is a replacement reagent in the<br>Kallestad Fluorescent<br>Autoantibody test with mouse<br>kidney, mouse stomach/kidney,<br>Hep-2 cell line, or Crithidia luciliae<br>substrates. |
| Matrix | Human Serum | Human Serum |
| Storage<br>(Unopened) | 2°C to 8°C<br>until expiration date | 2°C to 8°C<br>until expiration date |
| Form | Liquid | Liquid |

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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized caduceus, which is a symbol often associated with medicine and healthcare. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the caduceus. The logo is black and white.

JAN 1 5 2003

Food and Drug Administration 2098 Gaither Road Rockville MD 20850

Ms. Yvette Lloyd Senior Regulatory Affairs Specialist Bio-Rad Laboratories, QSD 9500 Jeronimo Road Irvine, California 92618-2017

Re: k024224

> Trade/Device Name: LiquichekTM Anti-Smooth Muscle Control, Positive Regulation Number: 21 CFR § 866.5120 Regulation Name: Anti-Smooth Muscle Antibody, Indirect Immunofluorescent, Antigen, Control Regulatory Class: II Product Code: DBE Dated: December 20, 2002 Received: December 23, 2002

Dear Ms. Lloyd:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and 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) that do not require approval of a premarket approval application (PMA). 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 (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. In addition, FDA may publish further announcements concerning your device in the Federal Register.

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Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Parts 801 and 809); and good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820). This letter will allow you to begin marketing your device as described in your Section 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 information about the application of labeling requirements to your device, or questions on the promotion and advertising of your device, please contact the Office of In Vitro Diagnostic Device Evaluation and Safety at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer 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 Sutman

Steven I. Gutman, M.D., M Director Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health

Enclosure

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K024224 510 (k) Number (if known):

Liquichek™ Anti-Smooth Muscle Control, Positive Device Name:

Indications for Use:

The new Liquichek™ Anti-Smooth Muscle Control, Positive, is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing for the detection of smooth muscle autoantibodies.

(PLEASE DO NOT WRITE BELOW THE LINE-CONINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription use

or
Over-the Counter use

I. Pleeves for J. Bantista
(Division Sign-Off)
Division of Clinical Laboratory Devices

510(k) Number K024224