PRE-FILLED SYRINGE FOR KOALA IUP by CLINICAL INNOVATIONS, INC.

The pre-filled Syringe is 10 cc syringe filled with 0.9% isotonic saline and is an accessory to the Koala Intrauterine Pressure System used in priming the catheter. This product is a sterile, single-use device.

AI/ML Overview

This submission is for a medical device (pre-filled syringe) and does not involve AI/ML. Acceptance criteria and study details as requested for AI/ML devices are not applicable.

Here's a summary of the information provided in the document:

Device: Pre-filled Syringe for Koala Intrauterine Pressure Catheter

Intended Use: To prime the catheter in an intrauterine pressure monitoring system.

Predicate Devices: Pre-filled syringes used with the Medex MX 4042 Series Intrauterine Pressure Catheter and the Quest (formerly Healthdyne Cardiovascular) ISOFLO Intrauterine Pressure Monitoring & Amnio.

Basis for Substantial Equivalence:

Same intended uses: Priming catheters in intrauterine pressure monitoring.
Same basic technological characteristics: A syringe pre-filled with saline.
Same or similar materials: All materials are biocompatible and function well in the intended application.

Safety and Effectiveness Documentation:

Safety and effectiveness are similar to existing devices as demonstrated in the laboratory.
Biocompatibility testing shows that the materials used in the pre-filled syringe are safe for this application.
Effectiveness is stated to be the same as the predicate devices.

Regulatory Classification: Class II, 21 CFR §884.2700, Product code: 85 HFN.

Note: The document is a 510(k) summary for a relatively simple medical device (a pre-filled syringe). It primarily focuses on demonstrating substantial equivalence to predicate devices based on intended use, technological characteristics, and materials, rather than detailed performance metrics or clinical study data typically associated with more complex or AI-driven devices. Therefore, many of the specific questions regarding acceptance criteria and studies (e.g., sample size for test/training sets, expert consensus, MRMC studies, standalone performance for AI) are not applicable to this type of submission.

Summary

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Section 6.0 510(k) Summary

K973746

P191

NOV 2 4 1997

510(k) Summary

Submitter: Clinical Innovations, Inc. Name: Wm. Dean Wallace Address: 6477 So. Cottonwood St., Murray, UT 84107 Telephone: (801) 268-8200 Fax: (801) 266-7373

Proprietary Name: Common/Usual Name: Classification Name:

Intrauterine Pressure Monitor and Accessories Monitor, Pressure, Intrauterine

The legally marketed devices to which equivalence is claimed are the pre-filled syringes used with the Medex MX 4042 Series Intrauterine Pressure Catheter and the Quest (formerly Healthdyne Cardiovascular) ISOFLO Intrauterine Pressure Monitoring & Amnio.

Description of the device: The pre-filled Syringe is 10 cc syringe filled with 0.9% isotonic saline and is an accessory to the Koala Intrauterine Pressure System used in priming the catheter. This product is a sterile, single-use device.

Intended use: This accessory is used with a Koala Intrauterine Pressure System and is used in priming the catheter.

The pre-filled syringe is substantially equivalent to the predicate device because:

It has the same intended uses, namely, to prime the catheter in intrauterine pressure monitoring,
It has the same basic technological characteristics as predicate devices, namely, it is a syringe pre-filled with saline, and
It uses the same or similar materials, all of which have been shown to be biocompatible and to function well in the intended application.

The safety and effectiveness are similar to existing devices as demonstrated in the laboratory. Biocompatibility testing shows that the materials used in the pre-filled syringe are safe for this application. Effectiveness is the same as the predicate devices.

Wm. Dean Wallace, M.D., Ph.D.

10-6-97
Date

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Image /page/1/Picture/0 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with its wings spread, facing to the right. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

NOV 2 4 1997

Wm. Dean Wallace, M.D., Ph.D. President Clinical Innovations 6477 S. Cottonwood Street Murray, Utah 84107

Re: K973746

Pre-filled Syringe for Koala Intrauterine Pressure Catheter Dated: September 29, 1997 Received: October 1, 1997 Regulatory class: II 21 CFR §884.2700/Product code: 85 HFN

Dear Dr. Wallace:

We have reviewed your Section 510(k) notfication of intent to market the device and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, 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 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 requirement, as set forth in the Ouality System Regulation (OS) 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 Radiation Control provisions, or other Federal laws or regulations.

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 (301) 594-4613. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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 (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,

W.Liau Yu

Lillian Yin, Ph.D. Director, Division of Reproductive, Abdominal, Ear, Nose and Throat. and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications For Use 11.0

Device Name: Pre-filled Syringe for Koala Intrauterine Pressure Catheter

510(k) Number: K973746

Intended use: This accessory is used with a Koala Intrauterine Pressure System and is used in priming the catheter.

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

Concurrence of CDRH, Office of Device Evaluation (ODE)

Ryker R. Satling/
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number K973746

Prescription Use
(Per 21 CFR 801.109) ✓

Over-The-Counter Use

(Optional Format 1-2-96)

Regulation Number and Section

§ 884.2700 Intrauterine pressure monitor and accessories.

(a)
Identification. An intrauterine pressure monitor is a device designed to detect and measure intrauterine and amniotic fluid pressure with a catheter placed transcervically into the uterine cavity. The device is used to monitor intensity, duration, and frequency of uterine contractions during labor. This generic type of device may include the following accessories: signal analysis and display equipment, patient and equipment supports, and component parts.(b)
Classification. Class II (performance standards).