← Product Code [LZG](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/LZG) · K122483 # PEARL DIABETES MANAGEMENT SYSTEM (K122483) _Asante Solutions, Inc. · LZG · Jan 3, 2013 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/LZG/K122483 ## Device Facts - **Applicant:** Asante Solutions, Inc. - **Product Code:** [LZG](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/LZG.md) - **Decision Date:** Jan 3, 2013 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 880.5725 - **Device Class:** Class 2 - **Review Panel:** General Hospital - **Attributes:** Therapeutic ## Indications for Use The Pearl Diabetes Management System is intended for continuous, subcutaneous delivery of insulin at programmable basal and bolus rates for the management of diabetes mellitus in adult patients requiring insulin. ## Device Story Pearl Diabetes Management System is a continuous, programmable insulin delivery system for adult patients with diabetes. System components include a controller unit with a user interface for programming basal and bolus delivery parameters, a single-use pump body containing the drive mechanism and battery, and an infusion set adapter. The device operates by applying controlled force to a pre-filled insulin cartridge to deliver insulin via an infusion set. Used in clinical or home settings, the device is operated by the patient or healthcare provider. Output consists of automated insulin delivery based on programmed settings, allowing for precise glycemic management. The system is a modification of the previously cleared Pearl System, maintaining the same fundamental drive mechanism and microprocessor-based controller. ## Clinical Evidence Bench testing only. No clinical data provided. Performance verification included accuracy testing, altitude and altitude shock, free fall, liquid ingress, positive and negative elevation, system occlusion, and software validation. ## Technological Characteristics Continuous subcutaneous insulin infusion (CSII) pump. Components: controller, single-use pump body, infusion set adapter. Drive mechanism: electromechanical plunger drive. Control: microprocessor-based. Connectivity: not specified. Power: battery-operated. Software: embedded controller firmware. ## Regulatory Identification An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm. ## Predicate Devices - Pearl Diabetes Management System ([K100567](/device/K100567.md)) ## Reference Devices - Animas IR1200 ([K032257](/device/K032257.md)) - D-TRONplus ([K043000](/device/K043000.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ # K 122483 Image /page/0/Picture/1 description: The image shows a logo with a stylized design. The logo features a circular element with abstract shapes inside, resembling a stylized letter or symbol. Below the logo, there is some text, but it is too blurry to read clearly. The overall design appears modern and minimalist. Asante Solutions Inc. Pearl™ Diabetes Management System Special 510(k) August 10, 2012 510(k) Summary Section 1.2 ## Submitter Information # JAN 0 3 2013 | Company: | Asante Solutions | |---------------|----------------------------| | | 352 East Java Drive | | | Sunnyvale, CA 94089 | | | (408) 716-5600 | | | Robin Bush | | | Regulatory Project Manager | | Summary Date: | August 10, 2012 | # Name and Classification | Common Name: | Insulin Infusion Pump | |----------------------|-----------------------------------| | Proprietary Name: | Pearl™ Diabetes Management System | | Classification Name: | Pump, Infusion, Insulin | | Product Code: | LZG | | Regulation Number: | 880.5725 | | Class: | II | ## Predicate Devices The Pearl Diabetes Management System has the same intended use as a number of commercially available medical devices, operates within an established range of insulin delivery, and uses existing established technology also known as Continuous Subcutaneous Insulin Infusion (CSII). - Pearl Diabetes Management System (#K100567, Asante Solutions) a) ## Reference Devices - Animas IR1200 (#K032257, Animas Corporation) a) - D-TRONplus (K043000, Disetronic) b) {1}------------------------------------------------ #### Intended Use The Pearl Diabetes Management System is intended for continuous, subcutaneous delivery of insulin at programmable basal and bolus rates for the management of diabetes mellitus in adult patients requiring insulin. #### Description of Device The Pearl Diabetes Management System is a continuous, programmable insulin delivery system. It consists of a controller, a single use pump body and an infusion set adapter. The controller unit has a user interface to program delivery parameters for basal and bolus insulin delivery. It attaches to the pump body. The pump body provides the drive mechanism and battery power and holds the pre-filled insulin cartridges. The infusion set adapter is the conduit from the insulin cartridge to the final delivery tubing. #### Summary of Technological Characteristics The system uses existing established and unchanged technology and materials, relative to the previously cleared device. The system employs the same drive mechanism as that of the cleared Pearl System (#K100567) to apply controlled and accurate force to move the plunger in the insulin cartridge. The microprocessor based controller is unchanged. #### Performance Testing The system has been verified for performance and functionality to provide assurance that the device modifications have been designed and tested to assure conformance to the requirements for its intended use. The following are the major tests that were performed on the Pearl Pump System to support the modifications: - . accuracy - altitude and altitude shock . - . free fail - . liquid ingress - positive and negative elevation . - system occlusion . - software validation . {2}------------------------------------------------ #### Conclusion Performance testing on the modified device demonstrated that the Pearl Diabetes Management System performs reliably and delivers insulin as intended through the Asante Infusion Sets, and is safe for its intended use. Design verification testing confirmed that no new questions of safety or effectiveness were identified during device testing of the modified device. Based upon the successful safety and performance tests and the similarities to predicate device, the modified Pearl Diabetes Management System is substantially equivalent to the predicate Pearl System in design, features, performance, fundamental scientific technology, and indications for use. {3}------------------------------------------------ #### DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three lines representing its body and wings. The eagle is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES-USA" in a circular arrangement. #### Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 January 3, 2013 Mr. Robin Bush Project Manager, Regulatory Affairs Asante Solutions, Incorporated 352 East Java Drive SUNNYVALE CA 94089 Re: K122483 Trade/Device Name: Pearl™ Diabetes Management System Regulation Number: 21 CFR 880.5725 Regulation Name: Infusion Pump Regulatory Class: II Product Code: LZG Dated: December 18, 2012 Received: December 18, 2012 Dear Mr. Bush: 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {4}------------------------------------------------ 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 Part 801); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely yours. Anthong La m Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ Asante Solutions Inc. Pearl" Diabetes Management System Special 510(k) August 10, 2012 Indications for Use Section 1.1 510(k) Number: . asante 4122483 Device Name: Pearl™ Diabetes Management System Indications for Use: The Pearl Diabetes Management System is indicated for the continuous subcutaneous delivery of insulin at programmable basal and bolus rates for the management of diabetes mellitus in adult patients requiring insulin. Prescription Use ﮯ (Part 21 CFR 801 Subpart D) Over-The-Counter Use _ (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) and/or Concurrence of CDRH, Office of Device Evaluation (ODE) | (Division Sign-Off) | |----------------------------------------------| | Division of Anesthesiology, General Hospital | | Infection Control, Dental Devices | | 510(k) Number: | K122483 | |----------------|---------| |----------------|---------| | Keith G. Marin |
Digitally signed by Keith G. Marin
DN: c=US, o=U.S. Government,
ou=HHS, ou=FDA, ou=People,
cn=Keith G. Marin,
0.9.2342.19200300.100.1.1=00112
50397
Date: 2013.01.03 16:07:51 -05:00
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