Who is the manufacturer of iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask?

Sleepnet Corporation filed the 510(k) submission for iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask (K241469).

What is the FDA product code for iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask?

BZD. It is classified under 21 CFR 868.5905 as a Class 2 device in the Anesthesiology panel.

What is the regulatory pathway for iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask?

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

Who can help prepare an FDA 510(k) submission like iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask?

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.

iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask

K241469 · Sleepnet Corporation · BZD · Jun 15, 2024 · Anesthesiology

Device Facts

Record ID	K241469
Device Name	iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask
Applicant	Sleepnet Corporation
Product Code	BZD · Anesthesiology
Decision Date	Jun 15, 2024
Decision	SESE
Submission Type	Special
Regulation	21 CFR 868.5905
Device Class	Class 2
Attributes	Therapeutic

Indications for Use

The iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask are intended to be used with positive airway pressure devices, such as CPAP or bi-level, operating at 3 cmH2O to 30 cmH2O. The masks are to be used on adult patients (>30 kg) for whom positive airway pressure therapy has been prescribed. The masks are intended for single-patient multi-use in the home, hospital or institutional environment.

Device Story

Nasal vented masks (iQ 2, Phantom 2) provide interface between positive airway pressure device (CPAP/bi-level) and patient; deliver pressurized air (3-30 cmH2O) to nose; feature exhalation port for CO2 flushing. Used in home, hospital, or institutional settings by adult patients. Device is passive; connects to standard 22mm circuits. Includes magnets in headgear clips (380mT field strength). Healthcare providers prescribe therapy; patients self-administer. Output is pressurized air delivery; mask seal ensures therapy efficacy. Benefits include non-invasive respiratory support. Updated labeling includes contraindications and warnings regarding magnetic field interactions with medical implants.

Clinical Evidence

No clinical data. Bench testing only. Performance data (exhaust flow, dead space, resistance to flow, sound levels) and biocompatibility/reprocessing data from the predicate device were leveraged as the subject device design is identical.

Technological Characteristics

Nasal vented mask with gel bladder, mask shell, and headgear. Standard 22mm connection. Passive device; no energy source. Materials identical to predicate. Magnetic headgear clips (380mT). Non-sterile. Single-patient multi-use. Shelf life 5 years.

Indications for Use

Indicated for adult patients (>30 kg) prescribed positive airway pressure therapy (CPAP or bi-level) at 3-30 cmH2O. Contraindicated for patients or individuals in close physical contact with the mask who have active medical implants or metallic implants that interact with magnets (e.g., pacemakers, ICDs, neurostimulators, aneurysm clips, stents, ocular implants, insulin pumps, CSF shunts, embolic coils, metallic splinters, cochlear implants, flow disruption devices, contact lenses with metal, dental implants, metallic cranial plates, screws, burr hole covers, bone substitutes, or magnetic implants/valves in upper limbs/torso).

Regulatory Classification

Identification

A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing.

Predicate Devices

Sleepnet iQ 2 and Phantom 2 Nasal Mask (K211274)

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food & 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 15, 2024 Sleepnet Corporation % Paul Dryden President ProMedic Consulting LLC 131 Bay Point Dr NE St. Ptersburg, Florida 33704 Re: K241469 Trade/Device Name: iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask Regulation Number: 21 CFR 868.5905 Regulation Name: Noncontinuous Ventilator (IPPB) Regulatory Class: Class II Product Code: BZD Dated: May 23, 2024 Received: May 24, 2024 Dear Paul Dryden: 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. 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" {1}------------------------------------------------ (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 OS 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 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-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 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. 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-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about mediation-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. ### Rachana Visaria -S Rachana Visaria, Ph.D. Assistant Director DHT1C: Division of Sleep Disordered Breathing, Respiratory and Anesthesia Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices {2}------------------------------------------------ Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ # Indications for Use 510(k) Number (if known) K241469 Device Name iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask Indications for Use (Describe) The iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask are intended to be used with positive airway pressure devices, such as CPAP or bi-level, operating at 3 cmH2O to 30 cmH2O. The masks are to be used on adult patients (>30 kg) for whom positive airway pressure therapy has been prescribed. The masks are intended for single-patient multi-use in the home, hospital or institutional environment. | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------|--| | | | | ☒ Prescription Use (Part 21 CFR 801 Subpart D) | ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | |------------------------------------------------|-----------------------------------------------| |------------------------------------------------|-----------------------------------------------| #### 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." {4}------------------------------------------------ | Sponsor: Sleepnet Corporation 5 Merrill Industrial Drive Hampton, NH 03842 | Tel - 603-758-6625 | |-------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------| | Sponsor Contact: | Jennifer Kennedy - Director of Regulatory and Quality | | Submission Correspondent: | Paul Dryden ProMedic, LLC | | Proprietary or Trade Name: | iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask | | Common/Usual Name: | Patient interface for CPAP | | Regulation Number: Regulation Code: Product Code: | 21CFR 868.5905 Non-continuous ventilator (IPPB) BZD | | Device: | iQ 2 and Phantom 2 Nasal Vented Mask | | Predicate Device: Regulation Number: Regulation Code: Product Code: | K211274 - Sleepnet iQ 2 and Phantom 2 Nasal Mask 21CFR 868.5905 Non-continuous ventilator (IPPB) BZD | #### Device Description: The Sleepnet iQ 2 and Phantom 2 Nasal Vented masks are nearly identical to the Predicate Sleepnet iQ 2 and Phantom 2 Nasal Mask (K211274). The subject of this submission is: · Addition of a contraindication related to magnets on the iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask • Update to the warning related to magnets on the iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask #### Indications for Use: The iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask are intended to be used with positive airway pressure devices, such as CPAP or bi-level, operating at 3 cmH2O to 30 cmH2O. The masks are to be used on adult patients (>30 kg) for whom positive airway pressure therapy has been prescribed. The masks are intended for single-patient multi-use in the home, hospital or institutional environment. Patient Population: For adults (>30 kg) Environment of Use: Home or hospital / institutional environments Substantial Equivalence Discussion: {5}------------------------------------------------ The Sleepnet iQ 2 and Phantom 2 Nasal Vented masks are viewed as substantially equivalent to the predicate device because: #### Indications - - We have updated the device name and removed "or above" in the Indications for Use which are similar. - Similar to the predicate - K211274. #### Patient Population - - The masks are to be used on adult patients (>30 kg) for whom positive airway pressure ● therapy has been prescribed. - Identical to the predicate K211274. ● #### Environment of Use - - The masks are intended for use in the home or hospital/institutional environment. - Identical to the predicate K211274. ● #### Technological Characteristics - - Identical technology to the predicate K211274. ● #### Non-Clinical Testing Summary - #### Bench testing - No new performance testing was conducted on the subject device, since the device designs are identical to the predicates. Discussion - The performance test results from the predicate device were leveraged for the subject device. #### Biocompatibility - There has been no change in the materials – the subject and predicate device utilize the same materials. Discussion - The biocompatibility test results from the predicate device were leveraged for the subject device. #### Reprocessing - There has been no change in the reprocessing - the subject and predicate device utilize the same reprocessing instructions. Discussion - The reprocessing test results from the predicate device were leveraged for the subject device. We have demonstrated that the proposed device is equivalent to the predicate, K211274. {6}------------------------------------------------ # K241469 510(k) Summary Page 3 of 7 15-Jun-24 # Table of Comparison to Predicate | Attributes | Subject - iQ 2 Nasal Vented Mask and | Predicate - iQ 2/ Phantom 2 Nasal Mask | Explanation of Differences | |--------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------| | | Phantom 2 Nasal Vented Mask | | | | 510(k) | K241469 | K211274 | | | Product Classification CFR | BZD CFR 868.5905 | BZD CFR 868.5905 | Identical | | Indications for Use | The iQ 2 Nasal Vented Mask and Phantom 2 Nasal Vented Mask are intended to be used with positive airway pressure devices, such as CPAP or bi-level, operating at 3 cmH2O to 30 cmH2O. The masks are to be used on adult patients (>30 kg) for whom positive airway pressure therapy has been prescribed. The masks are intended for single-patient multi-use in the home, hospital or institutional environment. | The iQ 2/ Phantom 2 Nasal Mask is intended to be used with positive airway pressure devices, such as CPAP or bi-level, operating at or above 3 cm H2O. The mask is to be used on adult patients (>30kg) for whom positive airway pressure therapy has been prescribed. The mask is intended for single- patient multi-use in the home, hospital or institutional environment. | Similar Removed "or above" for clarity | | Patient Population | Adult (>30 kg) | Adult (>30 kg) | Identical | | Patient type | Patients for whom positive airway pressure therapy has been prescribed | Patients for whom positive airway pressure therapy has been prescribed | Identical | | Prescriptive | Yes | Yes | Identical | | Principle of Operation | Device provides a seal over the nose to allow for delivery of pressurized air from a positive airway pressure device. Device has an exhalation port for flushing out exhaled CO2. The device is passive until connected to the positive pressure device. | Device provides a seal over the nose to allow for delivery of pressurized air from a positive airway pressure device. Device has an exhalation port for flushing out exhaled CO2. The device is passive until connected to the positive pressure device. | Identical | | Contraindication and Warnings | New Contraindication Do not use this mask if you or anyone (example: household members, bed partners, caregivers, etc.) in close physical contact with your mask has an active medical implant or metallic implant that will interact with magnets. Implant examples include, but are not limited to, pacemakers, implantable | There were no contraindications in K211274. | New as per recall event #94169 Original K211274 labeling available in Section 006_Labeling. | | | | | | | | cardioverter defibrillators (ICD), neurostimulators, aneurysm clips, metallic stents, ocular implants, insulin/infusion pumps, cerebral spinal fluid (CSF) shunts, embolic coils, metallic splinter, implants to restore hearing or balance with implanted magnets (such as cochlear implants), flow disruption devices, contact lenses with metal, dental implants, metallic cranial plates, screws, burr hole covers, bone substitute device, magnetic metallic implants/electrodes/valves placed in upper limbs, torso, or higher, etc. If you have any questions regarding the implant, consult your physician or the manufacturer of your implant. Updated Warning Magnets are used in the mask and headgear clips with a field strength of 380mT. With the exception of the devices identified in the contraindication, ensure that the mask is kept at least 6 inches (approx.16 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. For instance, the functioning of implants may change, or implants may move within the body due to magnetic attraction/repulsion. This applies to you or anyone in close physical contact with your mask. | Magnet Warning Magnets are used in the swivel frame/tube set and the headgear clips. The magnetic field strength is 380 mT. Ensure that the magnets are kept at least 2.25 inches (6 cm) away from any active medical implant or medical device that can be impacted by the magnetic field (e.g., pacemaker, defibrillators, neurostimulators, cochlear implants, hearing aids) to avoid possible effects from localized magnetic fields | | | Therapy Pressure Range | 3 cm H2O to 30 cm H2O. | 3 cm H2O to 30 cm H2O. | Identical | | Anatomical site | Face (seals around nose) | Face (seals around nose) | Identical | | | | | | | User Interface to administer therapy | Masks have a standard 22mm connection that connects to 22mm CPAP/bi-level circuits. | Masks have a standard 22mm connection that connects to 22mm CPAP/bi-level circuits. | Identical | | Environment of Use | The masks are intended for use in the home or hospital/institutional environment. | The masks are intended for use in the home or hospital/institutional environment. | Identical | | Attributes | Subject - iQ 2/ Phantom 2 nasal vented mask | Predicate - iQ 2/ Phantom 2 nasal mask | Explanation of Differences | | Useful life | Mask cushion - 1 month Swivel frame/tube set - 3 months Headgear and magnetic clips – 6 months | Mask cushion - 1 month Swivel frame/tube set - 3 months Headgear and magnetic clips - 6 months | Identical | | Shelf life | 5 years. | 5 years. | Identical | | Non-sterile | Yes | Yes | Identical | | Cleaning methods | Mild Soap (such as Ivory) and warm water | Mild Soap (such as Ivory) and warm water | Identical | | Available sizes | 1 | 1 | Identical | | Shape | Identical | Identical | Identical | | Incorporates an Exhaust port | Yes | Yes | Identical | | Components of the mask | Mask cushion Mask shell Gel bladder Headgear Swivel frame/tube set (tubing assembly) | Mask cushion Mask shell Gel bladder Headgear Swivel frame/tube set (tubing assembly) | Identical | | Shell design | Soft | Soft | Identical | {7}------------------------------------------------ # K241469 510(k) Summary {8}------------------------------------------------ # K241469 510(k) Summary | Duration of Use | Single patient, multi-use | |-----------------|---------------------------| | | Single patient, multi-use | | | Identical | {9}------------------------------------------------ # K241469 510(k) Summary Page 6 of 7 15-Jun-24 | Attributes | Subject - iQ 2/ Phantom 2 nasal vented mask | | | Predicate - iQ 2/ Phantom 2 nasal mask | | | Explanation of Differences | |-----------------------------------------|------------------------------------------------------------------------------------------------------|------------------------|-----------|------------------------------------------------------------------------------------------------------|------------------------|-----------|----------------------------| | Patient Contact per ISO 10993-1 | Skin contact, Skin and Externally Communicating with tissue (air pathway) Permanent contact | | | Skin contact, Skin and Externally Communicating with tissue (air pathway) Permanent contact | | | Identical | | Exhaust Flow | Pressure (cm H2O) | Exhaust flow (lpm) | | Pressure (cm H2O) | Exhaust flow (lpm) | | Identical | | | | iQ 2 | Phantom 2 | | iQ 2 | Phantom 2 | | | | 4 | 18.2 | 18.9 | 4 | 18.2 | 18.9 | | | | 8 | 26.3 | 27.5 | 8 | 26.3 | 27.5 | | | | 12 | 34.3 | 35.2 | 12 | 34.3 | 35.2 | | | | 16 | 39.6 | 39.2 | 16 | 39.6 | 39.2 | | | | 20 | 44.0 | 45.3 | 20 | 44.0 | 45.3 | | | | 24 | 49.8 | 50.6 | 24 | 49.8 | 50.6 | | | | 28 | 53.4 | 55.3 | 28 | 53.4 | 55.3 | | | | 30 | 55.6 | 56.8 | 30 | 55.6 | 56.8 | | | Dead space | iQ 2 – Mask – 47.3 ml Tubing – 68.33 ml | | | iQ 2 – Mask – 47.3 ml Tubing – 68.33 ml | | | Identical | | | Phantom 2 – Mask – 30.7 ml Tubing – 68.33 ml | | | Phantom 2 – Mask – 30.7 ml Tubing – 68.33 ml | | | | | Resistance to flow (pressure drop) | Flow rate (lpm) | Pressure drop (cm H2O) | | Flow rate (lpm) | Pressure drop (cm H2O) | | Identical | | | | iQ 2 | Phantom 2 | | iQ 2 | Phantom 2 | | | | 50 | 0.45 | 0.45 | 50 | 0.45 | 0.45 | | | | 100 | 2.05 | 2.06 | 100 | 2.05 | 2.06 | | | Sound pressure and Sound power level | iQ 2 – Sound pressure - 30.32 dB Sound power - 33.33 dB | | | iQ 2 – Sound pressure - 30.32 dB Sound power - 33.33 dB | | | Identical | | | Phantom 2 – Sound pressure – 30.49 dB Sound power – 33.50 dB | | | Phantom 2 – Sound pressure – 30.49 dB Sound power – 33.50 dB | | | | {10}------------------------------------------------ # K241469 510(k) Summary Page 7 of 7 15-Jun-24 # Substantial Equivalence Conclusion: The iQ 2 Nasal Vented Mask and Phantom 2 Nasal Ventical indications, technological characteristics and principles of operation and performance to the predicate and performance testing demonstrates that the subject device is use the predicate.

iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask

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Indications for Use

Device Story

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iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask

Device Facts

Indications for Use

Device Story

Clinical Evidence

Technological Characteristics

Indications for Use

Regulatory Classification

Identification

Predicate Devices

Submission Summary (Full Text)

Panel 1

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Special Control Matches

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