Who is the manufacturer of AblatePal Radiofrequency Ablation System?

Compal Electronics, Inc. filed the 510(k) submission for AblatePal Radiofrequency Ablation System (K223135).

What is the FDA product code for AblatePal Radiofrequency Ablation System?

GEI. It is classified under 21 CFR 878.4400 as a Class 2 device in the General, Plastic Surgery panel.

What is the regulatory pathway for AblatePal Radiofrequency Ablation System?

510(k) clearance (submission type: Traditional).

What are the predicate devices for AblatePal Radiofrequency Ablation System?

Cool-tip™ RF Ablation System (K042216).

Who can help prepare an FDA 510(k) submission like AblatePal Radiofrequency Ablation System?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

AblatePal Radiofrequency Ablation System

K223135 · Compal Electronics, Inc. · GEI · Jun 30, 2023 · General, Plastic Surgery

Device Facts

Record ID	K223135
Device Name	AblatePal Radiofrequency Ablation System
Applicant	Compal Electronics, Inc.
Product Code	GEI · General, Plastic Surgery
Decision Date	Jun 30, 2023
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 878.4400
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The AblatePal Radiofrequency Ablation System is designed to provide monopolar radiofrequency (RF) energy to be used for coagulation and ablation of soft tissue. The device is a prescription device.

Device Story

Monopolar RF generator system for soft tissue coagulation and ablation; utilizes active electrodes and neutral electrodes. Input: user-defined settings (time, temperature, impedance) via touchscreen; RF current delivered from generator through active electrode to patient tissue; neutral electrode returns current to generator. Heat generated by tissue resistance enables ablation. Operated by clinicians in clinical settings. Includes footswitches for activation and power adjustment. Output: RF energy delivery; informational signals and alerts on touchscreen. Benefits: controlled tissue ablation. System includes generator, footswitches, power cord, and single-use electrode kits (active electrode, tubing, neutral electrodes).

Clinical Evidence

No clinical data. Evidence consists of bench testing and ex-vivo animal tissue studies (liver, kidney, muscle). Bench testing verified electrical safety, EMC, and ablation zone dimensions compared to predicate. Ex-vivo testing demonstrated equivalent histological, thermal, and ablative performance.

Technological Characteristics

Monopolar RF generator; 480kHz ±10% output frequency; 0-200W power output. Impedance monitor (25-1000 Ohm); temperature continuity monitor (10-99°C). Materials: Al alloy neutral electrodes. Connectivity: touchscreen interface, footswitch inputs. Sterilization: EtO (active electrodes). Software: Moderate level of concern. Complies with IEC 60601-1, 60601-1-2, 60601-2-2.

Indications for Use

Indicated for coagulation and ablation of soft tissue. Prescription use only.

Regulatory Classification

Identification

An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.

Predicate Devices

Cool-tip™ RF Ablation System (K042216)

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K193355 — Electrodes Handpieces for Mygen V-1000 RF System · RF Medical Co., Ltd. · Aug 3, 2020
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Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. June 30, 2023 Compal Electronics, Inc Casper Chen Senior Director No. 581, Ruiguang Rd., Neihu District Taipei City, 11492 Taiwan ## Re: K223135 Trade/Device Name: AblatePal Radiofrequency Ablation System Regulation Number: 21 CFR 878.4400 Regulation Name: Electrosurgical Cutting And Coagulation Device And Accessories Regulatory Class: Class II Product Code: GEI Dated: May 29, 2023 Received: June 1, 2023 ## Dear Casper Chen: 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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. 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 {1}------------------------------------------------ 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, Digitally signed by Mark Mark Trumbore -S Trumbore -S Date: 2023.06.30 15:38:18 -04'00' Mark Trumbore, Ph.D. Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K223135 Device Name AblatePal Radiofrequency Ablation System Indications for Use (Describe) The AblatePal Radiofrequency Ablation System is designed to provide monopolar radiofrequency (RF) energy to be used for coagulation and ablation of soft tissue. The device is a prescription device. | Type of Use (Select one or both, as applicable) | | |----------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------| | <div> ☑ Prescription Use (Part 21 CFR 801 Subpart D) </div> | <div> ☐ Over-The-Counter Use (21 CFR 801 Subpart C) </div> | #### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ #### 510(k) Summary #### 1. Date of Summary Preparation June 28, 2023 #### 2. 510(k) Submitter/Holder Compal Electronics, Inc. No. 581, Ruiguang Rd., Neihu Dist. Taipei, 11492, Taiwan (R.O.C.) #### 3. Contact: Casper Chen Senior Director of Medical Product Division Casper_Chen@compal.com Email: Address: No. 581, Ruiguang Rd., Neihu Dist. Taipei, 11492, Taiwan (R.O.C.) #### 4. Device | Device Trade Name: | AblatePal Radiofrequency Ablation System | |----------------------|----------------------------------------------------------------| | Device Common Name: | RF Ablation System | | Classification Name: | Electrosurgical Cutting and Coagulation Device and Accessories | | Regulation: | 21 CFR 878.4400 | | Regulatory Class: | II | | Product Code: | GEI | #### 5. Predicate Device The AblatePal Radiofrequency Ablation System is substantially equivalent to the following, commercially available predicate devices: | Device Name | Classification Name and Class | 510(k) Number(s) | |---------------------------------|------------------------------------------------------|---------------------------------------| | Cool-tip™ RF Ablation System | Electrosurgical, Cutting & Coagulation & Accessories | K042216 (Primary Predicate Device) | #### 6 Intended Use / Indications for Use The AblatePal Radiofrequency Ablation System is designed to provide monopolar radiofrequency (RF) energy to be used for coagulation and ablation of soft tissue. The device is a prescription device. {4}------------------------------------------------ ## 7. Device Description The AblatePal Radiofrequency Ablation System (subject device) (HFM01-MD2202) is a monopolar radiofrequency (RF) generator with dedicated components and accessories. The generator can be operated in only impedance mode that use various combinations of time, tissue temperature, tissue impedance, and manual control. An interactive touchscreen display allows user input to the generator and displays informational signals and alert messages. Active electrodes are placed in the tissue to deliver RF energy to the tissue to be ablated. Only one electrode can be attached to the generator and can be used individually. During the ablation of tissue, RF current flows from the generator to an active electrode which delivers the current to the patient. The RF current flows from the active electrode through the patient's body tissue to the Neutral Electrode, which recovers the current and returns it to the qenerator. The resistance to the current, provided by the patient's tissue, produces the heat that is necessary for ablation of tissue. The dedicated system components include: - o RF Generator, radiofrequency generator - . Ablation Foot Switch (HFM01-AF0002): Single Foot Switch. Pressing the foot switch that RF Generator starts or stops ablating. - . Power Control Foot Switch (HFM01-AF0001): Double Foot Switch. Pressing the foot switch to adjust power in whole units of Watts that the RF Generator will deliver during the ablation. The blue foot switch can increase the power, and the yellow foot switch can decrease the power. - . Power Cord (WS-001H+WS-002): A line cord that provides AC power to the RFA system. - Electrode Kit (HFM01-AC0001~ HFM01-AC0006), including radiofrequency electrode, inflowo outflow tubing sets and Neutral Electrodes (HFM01-AE0001). The generator is packaged individually and is always supplied with the accessory items: footswitch and cables. The electrode kit HFM01-AC0001~ HFM01-AC0006 is separately packaged. The following AblatePal Radiofrequency Ablation System compatible accessories are single use: - . Electrode Kit (HFM01-AC0001~ HFM01-AC0006), including a radiofrequency electrode, inflow-outflow tubing sets and Neutral Electrodes. #### 8. Comparison of Technological Characteristics with the Predicate Device The AblatePal Radiofrequency Ablation System (subject device) relies on the same principles of operation and has similar performance characteristics, with respect to its intended use, as the predicate devices. The AblatePal Radiofrequency Ablation System combines the functional characteristics of the predicate Cool-tip™ generator (K042216). {5}------------------------------------------------ There are three main differences between the AblatePal Radiofrequency Ablation System and the predicate Cool-tip™ RF Ablation System 1. New larger patient Neutral Electrode compared to the predicate device. 2. The generator combines the functional characteristics of the predicate Cool- tip™ generator into a single RF generator that includes a different user interface and software controls. 3. The addition of several optional accessories, specifically, footswitches. Unlike the predicate device, the AblatePal Radiofrequency Ablation System has only one category of RF Ablation electrodes (monopolar). The AblatePal Radiofrequency Ablation System active electrodes deliver RF energy from the AblatePal Radiofrequency Ablation System generator for the ablation of tissue when used with an irrigation pump, which must comply with IEC 60601-1, and electrode kits. An electrode kit with a single active electrode (sterile), inflow-outflow tubing sets (sterile) and two Neutral Electrodes (non-sterile) are available. All kit items are single use. | Description | Subject Device | Predicate Device | Comparison | |-----------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | AblatePal Radiofrequency Ablation System (K223135) | Cool-tip™ RF Ablation System (K042216) | | | Indications for Use | The AblatePal Radiofrequency Ablation System is designed to provide monopolar radiofrequency (RF) energy to be used for coagulation and ablation of soft tissue. The device is a prescription device. | The Valleylab Cool-tip RF System (generator and accessories) is intended for the use in percutaneous, laparoscopic, and intraoperative coagulation and ablation of tissue, such as partial or complete ablation of non-resectable liver lesions. | The indication of "percutaneous, laparoscopic, and intraoperative coagulation and ablation of tissue, such as partial or complete ablation of non-resectable liver lesions" has been removed from the subject device. | | Prescription or OTC | Prescription | Prescription | Same | | ESU • Major function | Monopolar impedance monitor: Range:25-1000 Ohm Resolution:1 Ohm Accuracy:50-200 Ohm (± 10%) continuity monitor: temperature Range: 10-99°C Resolution: 0.1°C Accuracy: ±4°C | Monopolar impedance monitor: Range:0-1000 Ohm Resolution:1 Ohm Accuracy:50-100 Ohm (± 10%), 500-1000 Ohm (± 20%) continuity monitor: temperature Range: 10-99°C Resolution: 1°C Accuracy: ±4°C | Same: Monopolar Impedance monitoring of the subject device is in the range of that of the predicate device Same: continuity monitor | | ESU • Performance specifications | Output frequency: 480kHz±10% Waveform: AC sin wave (110 V) | Output frequency: 480kHz±10% | Accuracy of the subject device is in the range of that of the | | | Power output: 0-200W Max 50 Ohm output load. Accuracy is ±20%. | Waveform: AC sin wave (100/120 V) | predicate device | | | Voltage output: 100Vrms at 50Ω in 200W | Power output: 0-200W Max 50 Ohm output load. Accuracy is ±15%. | Others are same | | | | Voltage output: 100Vrms at 50Ω in 200W | | | ESU • Physical specifications | 12.0 kg 39 x 32.5 x 22.5 cm | 8.0 kg 41.8 x 28.0 x 14.0 cm | ESU of the subjective device is heavier than that of the predicate device | | Active accessory • Monopolar or bipolar • Physical dimensions and design (e.g., size, | - Monopolar - Length: 10/15/20cm - Exposure: 0.5/1/2/3 cm - Diameter: 17/18 G - EO sterilization - Specification: 100V Vrms,2A | - Monopolar - Length: 10/14.4/15/20/25 cm - Exposure: 0.7/1/2/3/ cm - Diameter: 17G - EO sterilization - Specification: 100V Vrms,2A | Length, exposure, diameter of the subject device is in the range of that of the predicate device | | length, connector type) • Rated voltage • Materials (electrode, insulation, coating, etc.) | | | Others are same | | Neutral electrodes • Conductive or capacitive • Physical specifications • Materials | - Conductive - Material: Al alloy - Specification: 23x14 cm | - Conductive - Material: Al alloy - Specification: 22x13 cm | Neutral electrodes of the subjective device are larger than those of the predicate device | | Miscellaneous accessories • Functions | Ablation Foot Switch (Single Foot Switch): Pressing the foot switch that RF Generator starts or stops ablating. Power Control Foot Switch (Double Foot Switch): Pressing the foot switch to adjust power in whole units of Watts that the RF Generator will deliver during the ablation. The blue foot switch can increase the power, and the yellow foot switch can decrease the power. - Specification: 25VAC,5A | N/A | Addition of Ablation Foot Switch and Power Control Foot Switch. | | • Performance specifications • Physical specifications • Materials | | | Performance data is provided in HFM01-F- 24 System test report (section 20-22) and IEC 60601-2-2 report to support that, even with significant differences, the device is as safe and effective as the predicate. | {6}------------------------------------------------ {7}------------------------------------------------ ## 9. Performance Testing Non-clinical performance testing was performed, and reports are provided in support of substantial equivalence with the predicate device. #### 9.1 Summary of Bench Testing Electrical Safety and Electromagnetic Compatibility (EMC): Bench testing and verification were conducted to ensure proper device function. At the system level, electrical safety and electromagnetic compatibility were evaluated to establish conformity to the applicable IEC 60601 safety standards, as identified below. - o IEC 60601-1:2005/AMD1:2020 Medical Electrical Equipment Part 1 General Requirements for Basic Safety and Essential Performance - . IEC 60601-1-2:2021 Medical Electrical Equipment - Part 1-2: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Electromagnetic Disturbances - Requirements and Tests - IEC 60601-2-2:2017 Medical Electrical Equipment Part 2-2: Particular Requirements for the . Basic Safety and Essential Performance of High Frequency Surgical Equipment and High Frequency Surgical Accessories The performance and safety of the AblatePal Radiofrequency Ablation System was characterized using laboratory (bench) verification and simulated-use validation testing consisting of soft tissue performance providing a characterization of the AblatePal Radiofrequency Ablation System ablation performance across the complete range of modes, electrodes, and in three tissue types: liver, kidney, and muscle. Ablation performance verifying the equivalence between the predicate Cool-tip™ RFA System and AblatePal Radiofrequency Ablation System when used with the AblatePal Radiofrequency Ablation System was performed at the system level to demonstrate the following: {8}------------------------------------------------ - . AblatePal Radiofrequency Ablation System RF Ablation Generator meets all design and performance requirements necessary to prove substantial equivalence with the predicate device, - . AblatePal Radiofrequency Ablation System RF Ablation Generator meets all ablation performance design requirements and to demonstrate the ablations zone dimensions created with the AblatePal Radiofrequency Ablation System Ablation Generator (subject) and Cooltip™ RF Ablation Generator (predicate) are equivalent, - The AblatePal Radiofrequency Ablation System Neutral Electrode, and RF Ablation cable ● meet design and performance requirements, - o The AblatePal Radiofrequency Ablation System with Ablation Generator meets IEC, EMC. requlatory and safety requirements, - Validate the usability of AblatePal Radiofrequency Ablation System Ablation Generator (HFM01-MD2202) with the intended users, - The packaging of AblatePal Radiofrequency Ablation System, including RF Ablation Generator, Neutral Electrode, RF Ablation Electrode Kits, can provide protection during simulated transportation. #### 9.2 Animal Testing Ex-vivo testing conducted demonstrated the histological, thermal and ablative performance , as well as procedural safety of the subject device is equivalent to the predicate for the AblatePal Radiofrequency Ablation System intended use. #### 10. Software Software for the AblatePal Radiofrequency Ablation System was developed in accordance with FDA Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices, for devices with a Moderate Level of Concern. System level software testing was completed successfully. #### 11. Biocompatibility The direct patient contacting devices of the AblatePal Radiofrequency Ablation System are the Neutral Electrode and active electrode. These devices are disposable and intended for single use. These devices were assessed for biocompatibility and potential adverse health effects associated with patient contacting disposable devices and were determined to be acceptable. {9}------------------------------------------------ ## Direct Patient Contacting Devices: #### Neutral Electrode: The Neutral Electrode is used to collect the RF energy delivered at the active electrode and return it to thegenerator. The patient contacting materials in the Neutral Electrode were tested to thebiocompatibility requirements shown below. - Cytotoxicity - Sensitization - o Skin Irritation #### Active Electrode: Active electrodes are placed in the tissue to deliver RF energy to the tissue being ablated. The patient contacting materials in the Active Electrode were tested to the biocompatibility requirements shown below: - . Cytotoxicity - Sensitization ● - Intracutaneous reactivity - Acute Systemic Toxicity ● - Pyrogen ● #### 12. Sterilization and Shelf life The active electrodes are provided sterile with SAL of 10°, are intended for use within the sterile field, and are designed for single use only. #### Electrode kit: The AblatePal Radiofrequency Ablation System electrode kits, including active electrode and tubing sets, are sterilized with EtO to a sterility level of 10 °. The sterile packaging is labeled as sterile for 3 years immediately following the date of manufacturing. The single use neutral electrode are not provided sterile and have a shelf life of 1.5 years. {10}------------------------------------------------ #### 13. Conclusion The AblatePal Radiofrequency Ablation System (subject device) and Cool-tip™ RF Ablation System (predicate device) have equivalent power and ablation performance characteristics based on verification and validation testing, and pre-clinical studies. Verification testing of the optional accessories consisting of the footswitch was conducted for their use with the subject device. As a result, the AblatePal Radiofrequency Ablation System has been shown to be substantially equivalent to the predicate device and does not raise different questions of safety and effectiveness.