(28 days)
No
The description focuses on the mechanical and electronic control of the vacuum pump and solenoid, with user control via buttons and an LCD display. There is no mention of AI, ML, or any adaptive or learning algorithms.
No
The device is a breast pump, intended for expressing and collecting milk, which is a supportive function for lactation rather than a direct therapeutic intervention for a disease or condition.
No
Explanation: The device is described as a breast pump intended to express and collect milk, not diagnose any medical condition.
No
The device description explicitly details hardware components such as a motor, vacuum pump, solenoid, LCD display, buttons, and internal rechargeable batteries, indicating it is a physical medical device with integrated software, not a software-only device.
Based on the provided information, the Evolve breast pump is not an IVD (In Vitro Diagnostic) device.
Here's why:
- Intended Use: The intended use is to "express and collect milk from their breasts." This is a physical process performed on the body, not a test performed on a sample taken from the body to diagnose a condition.
- Device Description: The description details a mechanical device that uses vacuum to extract milk. It does not mention any components or processes related to analyzing biological samples.
- Lack of IVD Characteristics: The document does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples (blood, urine, tissue, etc.)
- Providing diagnostic information
- Using reagents or assays
- Measuring biomarkers
The device is clearly intended for a physical function related to lactation, not for in vitro diagnostic testing.
N/A
Intended Use / Indications for Use
The Evolve breast pump is intended to be used by lactating women to express and collect milk from their breasts.
Product codes
HGX
Device Description
The Evolve Breast Pump, the subject device, is an electrically powered breast pump from an external AC-DC power supply or internal, rechargeable batteries; the device is provided non-sterile. The subject device is a cordless version of the predicate device.
The Evolve Breast Pump is intended to be used by lactating women to express and collect mills from their breasts. Pumping can be performed on one breast (single pumping) or on both breasts of a lactating woman at the same time (double pumping). The breast pump is designed as a multi-user breast pump and is available as a cordless model powered by an internal, rechargeable Lithium Ion battery or an external AC-DC power supply.
The Evolve Breast Pump utilizes a DC-powered motor driving a reciprocating-type vacuum pump and an electromechanical solenoid which are controlled electronically to provide vacuum (suction) capability that extracts and collects milk from breasts of lactating women.
The Evolve Breast Pump has a backlit, LCD display. The subject device also has soft-touch buttons for the user to power the device on/off, switch between two different pumping modes - stimulation and expression – and to control vacuum speed and strength within each of the modes. Multiple vacuum speed and strength settings are available in both pumping modes.
The Evolve Breast Pump is intended for repeated use by multiple users in the home environment.
The Evolve Breast Pump requires Hygeia's Personal Accessory System for users to express and collect milk from their breasts.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Breasts
Indicated Patient Age Range
Lactating women
Intended User / Care Setting
Home environment
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The Evolve Breast Pump was tested to demonstrate it meets its performance specifications. The testing involved measurement of vacuum and cycles for minimum and maximum settings for both single and double pumping mode, and for stimulation and expression mode with the internal, rechargeable Lithium Ion battery to show battery energy capacity is sufficient to assure the subject device performs to its specifications were met and are within the required, acceptable ranges for pump operation, cycle rate, vacuum pressure, and battery operation time.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 884.5160 Powered breast pump.
(a)
Identification. A powered breast pump in an electrically powered suction device used to express milk from the breast.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image contains the logos of the Department of Health and Human Services and the Food and Drug Administration (FDA). The Department of Health and Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
March 18, 2020
Hygeia II Medical Group, Inc. Brett Nakfoor CEO 6241 Yarrow Drive Carlsbad, CA 92011
Re: K200406
Trade/Device Name: Evolve Breast Pump Regulation Number: 21 CFR 884.5160 Regulation Name: Powered Breast Pump Regulatory Class: II Product Code: HGX Dated: February 18, 2020 Received: February 19, 2020
Dear Brett Nakfoor:
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
1
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 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 (OS) 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 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,
for Sharon M. Andrews Director DHT3B: Division of Reproductive, Gynecology and Urology Devices OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K200406
Device Name
Evolve Breast Pump
Indications for Use (Describe)
The Evolve breast pump is intended to be used by lactating women to express and collect milk from their breasts.
| Type of Use (Select one or both, as applicable) | |
|---|---|
| | Prescription Use (Part 21 CFR 801 Subpart D)
|X | Over-The-Counter Use (21 CFR 801 Subpart C)
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510(K) SUMMARY - K200406
In accordance to CFR Title 21, Sec. 807.92 the following summary is provided.
SUBMITTER:
Hygeia II Medical Group, Inc. 6214 Yarrow Drive, Suite A Carlsbad, CA 92011 Phone: (714) 515-7571
PRIMARY CONTACT PERSON:
Brett Nakfoor CEO Hygeia II Medical Group (714) 515-7571
SECONDARY CONTACT PERSON:
John Conklin Product Development Hygeia II Medical Group (714) 515-7571
DATE PREPARED: March 12, 2020
Device Information
Trade Name: Evolve Breast Pump Common Name: Powered Breast Pump Classification Name: Powered Breast Pump Classification Panel: Obstetrics/Gynecology Classification Regulation: 21 CFR 884.5160 Device Class: Class II Product Code: HGX (Pump, Breast, Powered)
Predicate Device Information
Hygeia Evolve Breast Pump, K190465, October 18, 2019.
The predicate device has not been subject to a design-related recall.
4
Device Description
The Evolve Breast Pump, the subject device, is an electrically powered breast pump from an external AC-DC power supply or internal, rechargeable batteries; the device is provided non-sterile. The subject device is a cordless version of the predicate device.
The Evolve Breast Pump is intended to be used by lactating women to express and collect mills from their breasts. Pumping can be performed on one breast (single pumping) or on both breasts of a lactating woman at the same time (double pumping). The breast pump is designed as a multi-user breast pump and is available as a cordless model powered by an internal, rechargeable Lithium lon battery or an external AC-DC power supply.
The Evolve Breast Pump utilizes a DC-powered motor driving a reciprocating-type vacuum pump and an electromechanical solenoid which are controlled electronically to provide vacuum (suction) capability that extracts and collects milk from breasts of lactating women.
The Evolve Breast Pump has a backlit, LCD display. The subject device also has soft-touch buttons for the user to power the device on/off, switch between two different pumping modes - stimulation and expression – and to control vacuum speed and strength within each of the modes. Multiple vacuum speed and strength settings are available in both pumping modes.
The Evolve Breast Pump is intended for repeated use by multiple users in the home environment.
The Evolve Breast Pump requires Hygeia's Personal Accessory System for users to express and collect milk from their breasts.
Indications for Use
The Evolve breast pump is intended to be used by lactating women to express and collect milk from their breasts.
Comparison of Technological Characteristics
The Evolve Breast Pump has identical indications for use and the same fundamental technology as the legally marketed predicated device, the Evolve Breast Pump (K190465). The modification to the predicate device, subject to this submission, is the addition of an internal rechargeable Lithium lon battery to allow cordless operation of the breast pump.
A summary of the technological characteristics of the subject and predicate device are shown in the following table.
| | Evolve
K200406 | Evolve
(Predicate Version)
K190465 | Comment |
|-------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------|
| Indications for Use | The Evolve powered breast
pump is to be used by lactating
women to express and collect
milk from their breasts. | The Evolve powered breast
pump is to be used by lactating
women to express and collect
milk from their breasts. | Same |
| Environment of
Use | Home | Home | Same |
| User Interface - Controls | | | |
| User Control | State-dependent controls:
On-Off button
Stimulation and Expression
Mode button | State-dependent controls:
On-Off button
Stimulation and Expression
Mode button | Same |
| | Performance controls:
Strength and Speed adjustment
via buttons | Performance controls:
Strength and Speed adjustment
via buttons | |
| Visual Indicator | LCD
Backlit, liquid-crystal display | LCD
Backlit, liquid-crystal display | Same |
| Pumping Options | Single pumping
Double pumping | Single pumping
Double pumping | Same |
| Adjustable Suction
Level | Yes | Yes | Same |
| Adjustable Speed
Level | Yes | Yes | Same |
| Accessories | Personal Accessory Set:
• breast shield
• diaphragm
• valve
• tubing
• bottles
AC-DC power-adapter-cord | Personal Accessory Set:
• breast shield
• diaphragm
• valve
• tubing
• bottles
AC-DC power-adapter-cord | Same
All components and
accessories have been
cleared with predicate
device (K190465) |
| Cleaning | Breast pump - wipe with clean,
damp cloth
Tubing - replace if milk appears
in tubing
Breast pump kit and bottles -
wash and sanitize | Breast pump - wipe with clean,
damp cloth
Tubing - replace if milk appears
in tubing
Breast pump kit and bottles -
wash and sanitize | Same |
| Specifications | | | |
| Power Source | AC-DC 100 - 240 Vac adapter,
50/60 Hz | AC-DC 100 - 240 Vac adapter,
50/60 Hz | Same |
| Batteries | Internal, rechargeable
Lithium Ion battery | N/A | Subject device has
internal
Lithium Ion battery |
| Rechargeable
Battery
operation/charge
time | Operation time:
Approximately 120 Minutes
Charge time:
Approximately 180 Minutes | N/A | Subject device provides
ability to operate in
cordless configuration by
battery |
| Software/firmware | Yes | Yes | Same |
| Vacuum aggregate
type | Reciprocating pump | Reciprocating pump | Same |
| Vacuum
Regulation type | Electronic | Electronic | Same |
| Maximum vacuum
(mmHg) | -283 mmHg
(-20 mmHg) | -283 mmHg
(-20 mmHg) | Same |
| Vacuum range –
double and single
pumping (mmHg) | Stimulation
-75 to -175 mmHg
(±20 mmHg)
Expression
-140 to -283 mmHg
(±20 mmHg) | Stimulation
-75 to -175 mmHg
(±20 mmHg)
Expression
-140 to -283 mmHg
(±20 mmHg) | Same |
| Cycling Control
Mechanism | Electronic | Electronic | Same |
| Cycle Speed
Range
(Cycles/Minute =
CPM) | Stimulation
75 to 92 CPM
(±8 CPM)
Expression
32 to 49 CPM
(±8 CPM) | Stimulation
75 to 92 CPM
(±8 CPM)
Expression
32 to 49 CPM
(±8 CPM) | Same |
| Adjustable
Cycle Speed
Levels | Yes | Yes | Same |
| Backflow
protection | Yes, silicone diaphragm | Yes, silicone diaphragm | Same |
5
6
The differences in technological characteristics do not raise different questions of safety and effectiveness.
Summary of Performance Data
The Evolve Breast Pump complies with voluntary standards for electrical safety, electromagnetic compatibility, and use in the home environment.
The following performance data is provided in support of the substantial equivalence determination:
Risk/Hazard
-
. Risk Analysis in accordance with ISO 14971:2007 was used to assess impact of modifications to the device
Electrical Safety and Electromagnetic Compatibility (EMC) -
Electrical safety testing per IEC 60601-1:2005 (3rd Edition) with US deviations per . AAMI/ANSI ES60601-1:2005/(R)2012 and A1:2012 standard
-
Electromagnetic compatibility testing per IEC 60601-1-2: 2014 (4th edition) standard, ● Medical Electrical Equipment Part 1 - 2
Performance Testing
The Evolve Breast Pump was tested to demonstrate it meets its performance specifications. The testing involved measurement of vacuum and cycles for minimum and maximum settings for both single and double pumping mode, and for stimulation and expression mode
7
with the internal, rechargeable Lithium Ion battery to show battery energy capacity is sufficient to assure the subject device performs to its specifications were met and are within the required, acceptable ranges for pump operation, cycle rate, vacuum pressure, and battery operation time.
Conclusion
The performance testing demonstrates that the Evolve Breast Pump is substantially equivalent to the predicate device.