Ceribell Instant EEG Headset

K254033 · Ceribell, Inc. · GXY · Feb 9, 2026 · Neurology

Device Facts

Record IDK254033
Device NameCeribell Instant EEG Headset
ApplicantCeribell, Inc.
Product CodeGXY · Neurology
Decision DateFeb 9, 2026
DecisionSESE
Submission TypeAbbreviated
Regulation21 CFR 882.1320
Device ClassClass 2
AttributesPediatric

Intended Use

The Ceribell Instant EEG Headset is intended for use in routine clinical settings where rapid placement of a number of EEG electrodes is desired.

Device Story

Single-use, non-sterile, disposable EEG electrode array; includes elastic fabric headset with up to 20 passive Ag/AgCl electrodes. Each electrode features integrated reservoir with conductive electrolyte gel and scalp-contacting prongs for skin preparation. Device connects via integrated cable to external EEG acquisition/recording system. Used in routine clinical settings; operated by healthcare professionals. Collects scalp EEG signals; provides conductive bridge between scalp and recording equipment. Facilitates rapid EEG setup; enables clinical monitoring of brain activity.

Clinical Evidence

No clinical data. Bench testing only. Performance demonstrated via electrical characterization (AC impedance, DC offset, noise, bias current) per ANSI/AAMI EC12 and biocompatibility testing per ISO 10993-1, -5, -10, and -23. Conductive connection compliance verified per ANSI/AAMI ES 60601-1.

Technological Characteristics

Passive Ag/AgCl electrodes; conductive electrolyte gel; nylon/spandex blend fabric; thermoplastic elastomer (TPE); aluminum oxide powder; UV adhesive. Dimensions support head sizes 45.1cm–62.0cm. Connectivity via integrated cable to EEG recording device. Biocompatibility per ISO 10993. Electrical performance per ANSI/AAMI EC12. Single-use, non-sterile.

Indications for Use

Indicated for patients with head sizes 45.1 cm – 62.0 cm requiring rapid EEG electrode placement in routine clinical settings. Not intended for use in neonates/newborns.

Regulatory Classification

Identification

A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0} FDA U.S. FOOD & DRUG ADMINISTRATION February 9, 2026 Ceribell, Inc. Angela Lynch Regulatory Affairs Manager 360 N. Pastoria Ave. Sunnyvale, California 94085 Re: K254033 Trade/Device Name: Ceribell Instant EEG Headset Regulation Number: 21 CFR 882.1320 Regulation Name: Cutaneous Electrode Regulatory Class: Class II Product Code: GXY Dated: December 16, 2025 Received: December 16, 2025 Dear Angela Lynch: 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 (the 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 available 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. U.S. Food & Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993 www.fda.gov {1} K254033 - Angela Lynch Page 2 Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download). Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30, Design controls; 21 CFR 820.90, Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181). 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 device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reporting-combination-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 Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050. All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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-devices/medical-device-safety/medical-device-reporting-mdr-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/medical-devices/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-devices/device-advice-comprehensive-regulatory- {2} K254033 - Angela Lynch Page 3 assistance/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, Tushar Bansal -S Tushar Bansal, PhD Acting Assistant Director, Acute Injury Devices Team DHT5B: Division of Neuromodulation and Physical Medicine Devices OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3} | Indications for Use | | | | --- | --- | --- | | Please type in the marketing application/submission number, if it is known. This textbox will be left blank for original applications/submissions. | K254033 | ? | | Please provide the device trade name(s). | | ? | | Ceribell Instant EEG Headset | | | | Please provide your Indications for Use below. | | ? | | The Ceribell Instant EEG Headset is intended for use in routine clinical settings where rapid placement of a number of EEG electrodes is desired. | | | | Please select the types of uses (select one or both, as applicable). | ☑ Prescription Use (21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | ? | {4} ceribell # 510(k) Summary – K254033 ## 1. SUBMITTER Ceribell, Inc. 360 North Pastoria Avenue Sunnyvale, California 94085 Contact Person: Raymond Woo, PhD Chief Technical Officer Telephone: (800) 436-0826 E-mail: ray@ceribell.com Alternative Contact: Angela Lynch Regulatory Affairs Manager E-mail: angela.lynch@ceribell.com Date Prepared: February 5, 2026 ## 2. DEVICE Trade Name: Ceribell Instant EEG Headset Common Name: Cutaneous electrode Classification: Cutaneous electrode (21 CFR 882.1320) Device Class: II Product Code: GXY ## 3. PREDICATE DEVICE Primary: Ceribell Instant EEG Headband, K232052 Secondary: Ceribell Instant EEG Headcap, K223086 ## 4. DEVICE DESCRIPTION The Ceribell Instant EEG Headset is a single-use, non-sterile, disposable EEG electrode device that includes up to 20 EEG electrodes that are placed on the subject’s scalp. The headset is a prescription-use device intended to collect and provide EEG signals to an EEG recording or monitoring device. The Ceribell Instant EEG Headset includes the following components: - Elastic fabric headset - Electrode assemblies, each consisting of the following: - Passive silver/silver chloride (Ag/AgCl) electrode - Reservoir filled with conductive electrolyte gel {5} ceribell - Mechanism for dispensing gel onto patient scalp - Scalp-contacting prongs to prepare scalp for electrode contact - Cable attached to the headset to allow connection to an EEG acquisition/recording device # 5. INDICATIONS FOR USE The Ceribell Instant EEG Headset is intended for use in routine clinical settings where rapid placement of a number of EEG electrodes is desired. # 6. COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICES Compared to the predicate devices, the subject device has the same intended use, similar product design and the same product effectiveness as summarized in the following table. | Attribute | Primary Predicate Device Ceribell Instant EEG Headband (K232052) | Secondary Predicate Device Ceribell Instant EEG Headcap (K223086) | Subject Device Ceribell Instant EEG Headset | Comparison | | --- | --- | --- | --- | --- | | Classification Regulation | Class II per 21 CFR 882.1320, Cutaneous Electrode | Class II per 21 CFR 882.1320, Cutaneous Electrode | Same as both predicates. | Same | | Product Code | GXY, Electrode, cutaneous; GWQ, full-montage standard electroencephalograph | GXY, Electrode, cutaneous | Same as both predicates. | Same | | Intended Use | A single-use disposable headpiece with an integrated array of passive cutaneous electrodes that are applied to the patient's head to record EEG signals when connected to an EEG recording device. | A single-use disposable headpiece with an integrated array of passive cutaneous electrodes that are applied to the patient's head to record EEG signals when connected to an EEG recording device. | Same as both predicates. | Same | | Indications for Use | The Ceribell Instant EEG Headband is an electroencephalogram (EEG) electrode array intended for single patient use in the recording of EEGs. The Instant EEG Headband is intended for prescription use in the home, healthcare facility, or clinical research environment. | The Ceribell Instant EEG Headcap is intended for use in routine clinical settings where rapid placement of a number of EEG electrodes is desired. | The Ceribell Instant EEG Headset is intended for use in routine clinical settings where rapid placement of a number of EEG electrodes is desired. | The subject device and both predicate devices include the same intended use as passive cutaneous electrodes for EEG. The subject device indications for | {6} ceribell | Attribute | Primary Predicate Device Ceribell Instant EEG Headband (K232052) | Secondary Predicate Device Ceribell Instant EEG Headcap (K223086) | Subject Device Ceribell Instant EEG Headset | Comparison | | --- | --- | --- | --- | --- | | | | | | use is identical to the secondary predicate device. | | Intended Patient Population | Any patient within the head size range of 45.1cm – 62.0cm | Any patient within the head size range of 26.0cm – 66.0cm | Patients within the head size range of 45.1 cm – 62.0 cm. Not intended for use in neonates/newborns. | Same | | Environment of Use | Electrophysiological | Electrophysiological | Same as both predicates. | Same | | Type of Patient Contact | Contacts patient’s scalp | Contacts patient’s scalp | Same as both predicates. | Same | | Type of Use | Single use, non-sterile, disposable | Single use, non-sterile, disposable | Same as both predicates. | Same | | Device Description | Single use, non-sterile, disposable EEG electrode array consisting of: - Silver/silver-chloride (Ag/AgCl) electrodes - Plastic packet gel reservoirs pre-filled with conductive electrolyte gel - Integrated cable connector to connect to an EEG recording device - A spandex blend fabric headband to secure the electrodes to the patient | Single use, non-sterile, disposable EEG electrode array consisting of: - Silver/silver-chloride (Ag/AgCl) electrodes - Cable to connect to an EEG recording device - A spandex blend fabric headcap to secure the electrodes to the patient | Single use, non-sterile, disposable EEG electrode array consisting of: - Silver/silver-chloride (Ag/AgCl) electrodes - Plastic packet gel reservoirs pre-filled with conductive electrolyte gel - Integrated cable connector to connect to an EEG recording device - A spandex blend fabric headset to secure the electrodes to the patient | - The subject device and both predicate devices contain an integrated array of silver/silver-chloride (Ag/AgCl) electrodes intended to acquire EEG signals. - The subject device and the primary predicate contain pre-filled conductive electrolyte gel reservoirs integrated into each electrode. | | Principle of Operation | Appropriately sized headband is fit on the patient’s head. Hair is cleared from the electrode contact surface and the skin prepared for electrode connection. Electroconductive gel is applied to the scalp contact area, creating a conductive bridge from the scalp to the headband electrodes. The cable of the headband is connected to an EEG | Appropriately sized headcap is fit on the patient’s head. Electrodes and chin strap are attached to the headcap. Electroconductive gel is applied to the scalp contact area, creating a conductive bridge from the scalp to the headcap electrodes. The cable of the headcap is connected to an EEG acquisition/recording | Same as both predicates. | Same | 3 {7} ceribell | Attribute | Primary Predicate Device Ceribell Instant EEG Headband (K232052) | Secondary Predicate Device Ceribell Instant EEG Headcap (K223086) | Subject Device Ceribell Instant EEG Headset | Comparison | | --- | --- | --- | --- | --- | | | acquisition/recording device for recording of EEG signals. | device for recording of EEG signals. | | | | Number of Electrodes | Ten (10) electrodes. | Various configurations supporting between 9 and 19 electrodes. | Up to 20 electrodes. | The number of electrodes in the subject device is similar to the secondary predicate. | | Electrode Locations | The placement of the electrodes is according to the International 10-20 system of electrode placement or the American Electroencephalographic Society positioning system (10-10). The number of the electrodes in use is according to the needs of clinical practice. | The placement of the electrodes is according to the International 10-20 system of electrode placement or the American Electroencephalographic Society positioning system (10-10). The number of the electrodes in use is according to the needs of clinical practice. | Same as **both predicates**. | Same | | Available Sizes | Various sizes (overall head size range 45.1cm – 62.0cm) | Various sizes (overall head size range 26.0cm – 66.0cm) | Same as the **primary predicate**. | Same | | Patient-Contacting Materials | • Nylon/Spandex blend • Thermoplastic elastomer (TPE) • Aluminum oxide powder • UV adhesive • Electroconductive gel | • Nylon/Spandex blend • Thermoplastic elastomer (TPE) | • Nylon/Spandex blend • Thermoplastic elastomer (TPE) • Aluminum oxide powder • UV adhesive • Electroconductive gel | The subject device patient-contacting materials are the same. | | Biocompatibility | ISO 10993-1 ISO 10993-5 (Cytotoxicity) ISO 10993-10 (Sensitization) ISO 10993-23 (Irritation or Intracutaneous Reactivity) | ISO 10993-1 ISO 10993-5 (Cytotoxicity) ISO 10993-10 (Sensitization) ISO 10993-23 (Irritation or Intracutaneous Reactivity) | ISO 10993-1 ISO 10993-5 (Cytotoxicity) ISO 10993-10 (Sensitization) ISO 10993-23 (Irritation or Intracutaneous Reactivity) Attachment G of FDA’s 2023 Biocompatibility Guidance | Biocompatibility evaluations are the same and follow the FDA guidance document “Cutaneous Electrodes for Recording Purposes-Performance Criteria for Safety and Performance Based Pathway”, August 2020. | 4 {8} ceribell® | Attribute | Primary Predicate Device Ceribell Instant EEG Headband (K232052) | Secondary Predicate Device Ceribell Instant EEG Headcap (K223086) | Subject Device Ceribell Instant EEG Headset | Comparison | | --- | --- | --- | --- | --- | | Cable | 0.1m – 3.0m integrated cable | 0.1m – 3.0m integrated cable | Same as both predicates. | Same | | Electrical Performance | ANSI/AAMI EC12 • Average AC Impedance: ≤ 2 kΩ (individual pairs ≤ 3kΩ) • DC Offset Voltage: ≤ 100 mV • Combined Offset Instability and Internal Noise: ≤ 150 μV • Bias Current Tolerance: ≤ 100 mV | ANSI/AAMI EC12 • Average AC Impedance: ≤ 2 kΩ (individual pairs ≤ 3kΩ) • DC Offset Voltage: ≤ 100 mV • Combined Offset Instability and Internal Noise: ≤ 150 μV • Bias Current Tolerance: ≤ 100 mV | Same as both predicates. | Electrical performance evaluations are the same and follow the FDA guidance document “Cutaneous Electrodes for Recording Purposes-Performance Criteria for Safety and Performance Based Pathway”, August 2020. | | Electrical Connection Compliance | • Conductive Connection Compliance (Patient Leads or Patient Cables) per ES 60601-1 consensus standard • IEC 60601-1 clause 8.5.2.3 • 21 CFR 898.12 | • Conductive Connection Compliance (Patient Leads or Patient Cables) per ES 60601-1 consensus standard • IEC 60601-1 clause 8.5.2.3 • 21 CFR 898.12 | Same as both predicates. | Electrical connection compliance requirements are the same and follow the FDA guidance document “Cutaneous Electrodes for Recording Purposes-Performance Criteria for Safety and Performance Based Pathway”, August 2020. | The results of the completed evaluations and testing demonstrate that any differences do not raise different questions of safety and effectiveness, and the performance data demonstrate acceptable safety and performance compared to the predicate devices. 5 {9} ceribell® # 7. PERFORMANCE DATA In accordance with the FDA guidance document, “Cutaneous Electrodes for Recording Purposes- Performance Criteria for Safety and Performance Based Pathway”, issued on August 14, 2020, the following performance data were provided to demonstrate safety and efficacy in support of substantial equivalence determination. ## Electrode Characterization: - Electrical Performance per FDA-recognized consensus standard, ANSI/AAMI EC12 Disposable ECG Electrodes - AC Impedance - Offset Voltage - Combined offset instability and internal noise - Bias Current Voltage (DC Voltage Offset) - Shelf-Life per FDA-recognized consensus standards, ANSI/AAMI EC12 Disposable ECG Electrodes and IEC 60601-2-2 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 - Conductive Connection Compliance - The design of the subject device is in conformance with subclause 8.5.2.3 of FDA-recognized consensus standard, ANSI/AAMI ES 60601-1 Medical Electrical Equipment Part 1 – General requirements for basic safety and essential performance. ## Biocompatibility Evaluation: - Biocompatibility per ISO 10993-1, ISO 10993-5, ISO 10993-10, and ISO 10993-23. The biocompatibility of the subject device is also based on the use of skin-contacting, low biocompatibility risk materials with a long history of safe use in accordance with Attachment G of the FDA’s 2023 Biocompatibility Guidance. # 8. SUMMARY The Ceribell Instant EEG Headset has the same intended use as the predicate devices. The differences in technological characteristics do not raise different questions of safety and effectiveness, and the performance data demonstrate that the Ceribell Instant EEG Headset is substantially equivalent to the cleared predicate devices.
Innolitics
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