(377 days)
The Rumble Tuff Electric Breast Pump is an electrically powered single-user device used to express and collect milk from the breasts of lactating women. The device is not intended for hospital use.
The Rumble Tuff Electric Breast Pump is a powered Breast Pump. With different models, the Pumping can be performed on one breast or on both breasts at the same time; the Rumble Tuff Electric Breast Pump can be powered by 4 AA batteries, one 7.4V Li batteries or an AC Adapter provided with the pump. The pumping system consists of a diaphragm-type vacuum pump which is driven by a microcontroller controlled DC electric motor. Rumble Tuff Electric Breast Pump has five models; PA200S, PA201S, PA201D, PA203S, and PA203D. The suffix "S" stands for the model with single collection kit, and "D" stands for the model with dual collection kits. The user interface of PA200S uses 4 LEDs for indicating pumping cycle and uses a roller type adjuster for pumping level adjustment and indicating pumping level. Models PA201S, PA201D, PA203S, and PA203D all use the same user interface, a LCD screen for showing the pumping information; it also uses a roller type adjuster for pumping level adjustment. For all models, the user is able to control the cycle speed and vacuum level.
Given the provided document, the "acceptance criteria" and "study proving the device meets the acceptance criteria" pertain to the performance specifications of the medical device (Rumble Tuff Electric Breast Pump) and the testing conducted to demonstrate its performance and safety, primarily for substantial equivalence to predicate devices under a 510(k) submission.
Here's an analysis based on the provided text, formatted to address your specific points:
Since this document is a 510(k) summary for a breast pump, the "acceptance criteria" are the performance specifications and safety standards it must meet to be considered substantially equivalent to a legally marketed predicate device. The "study that proves the device meets the acceptance criteria" refers to the testing performed and summarized in the application to demonstrate these aspects.
1. A table of acceptance criteria and the reported device performance
The document provides the performance specifications for the Rumble Tuff Electric Breast Pump models. These are the reported device performance and implicitly serve as the acceptance criteria because the device is being presented as meeting these specifications for substantial equivalence.
| Performance Characteristic | Acceptance Criteria (New Device: Rumble Tuff Electric Breast Pump) |
|---|---|
| Pumping Suction (Single Pumping Models) | 115 - 250 mmHg (PA201S, PA203S)125 - 250 mmHg (PA200S) |
| Pumping Suction (Double Pumping Models) | 85 - 250 mmHg (PA201D, PA203D) |
| Suction Settings (Stimulation) | 8 Levels (PA201S, PA201D, PA203S, PA203D) |
| Suction Settings (Expression) | 8 Levels (PA201S, PA201D, PA203S, PA203D) |
| Adjustable Suction Level | Yes (All models) |
| Back Flow Protection | Yes (All models) |
| Let Down Function | Yes (All models) |
| Pumping Cycles (PA200S) | up to 1.67/sec |
| Pumping Cycles (PA201S) | Up to 1.83/sec |
| Pumping Cycles (PA203S) | Up to 1.11/sec |
| Pumping Cycles (PA201D, PA203D) | Up to 1.23/sec |
| Material Biocompatibility | Meets ISO 10993 standards (e.g., ISO 10993-5, ISO 10993-10) for direct and indirect patient contact. |
| Electrical Safety | Meets IEC 60601-1:2005 |
| Electromagnetic Compatibility (EMC) | Meets IEC 60601-1-2:2007 |
2. Sample sized used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)
The document states, "Additionally, the tests of vacuum levels and cycle speeds conducted by Acute Ideas are provided to demonstrate the performance of Rumble Tuff Electric Breast Pump."
- Sample Size: The specific sample size for performance testing (e.g., number of units tested for vacuum levels and cycle speeds) is not specified in this document.
- Data Provenance: The tests were "conducted by Acute Ideas," which is based in Taipei, Taiwan. The document does not explicitly state whether the testing was prospective or retrospective, but typically, performance verification testing for a new device submission would be prospective.
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)
This document describes a medical device's performance validation (a breast pump), not an AI algorithm requiring expert ground truth for interpretation (like medical images). Therefore, this question is not applicable in the context of this device and submission. Performance is measured against physical specifications and international safety standards, not expert consensus on qualitative data.
4. Adjudication method (e.g. 2+1, 3+1, none) for the test set
Not applicable for device performance testing, which involves objective measurements against specifications rather than subjective interpretation requiring adjudication.
5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance
Not applicable. This is a breast pump, not an AI-assisted diagnostic device where MRMC studies are relevant.
6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done
Not applicable. This is a physical medical device, not an algorithm. Performance is inherent to the device's mechanical and electrical functions.
7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.)
The "ground truth" for this device primarily relies on objective physical measurements (e.g., vacuum pressure, cycle speed) against established engineering and medical device standards (e.g., IEC 60601-1, ISO 10993) and comparison to the performance of predicate devices. There is no qualitative "ground truth" in the diagnostic sense.
8. The sample size for the training set
Not applicable. This is not a machine learning or AI device that requires a training set.
9. How the ground truth for the training set was established
Not applicable as there is no training set for this type of device.
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Acute Ideas Co., Ltd.
3F, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan
3F, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan
Sr, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan
TEL: 886-2-8751 4868 FAX: 886-2-8751 5868
NOV 2 0 2012
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510(K) Summary
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| Applicant: | Acute Ideas Co., Ltd. |
|---|---|
| 3F, No. 11, Lane 35, Jihu Road, | |
| Neihu Dist, Taipei, Taiwan, 114, R.O.C. | |
| Tel: 886-2-87514868 | |
| Fax: 886-2-87515868 | |
| www.acuteideas.com | |
| Attn: Jessica Wang | |
| Contact: | Matthew Kho |
| A Cute Baby, Inc. | |
| 865 N 1430 W | |
| Orem UT 84057 USA | |
| Tel: 801.609.8168 | |
| Fax: 801.796.2688 | |
| Date of Submission: | 11/01/2012 |
| Proprietary Name: | Rumble Tuff Electric Breast Pump |
| (Models: PA200S, PA201S, PA201D, PA203S and PA203D) | |
| Common Name: | Electric Breast Pump |
| Classification name: | Pump, Breast, Powered |
| Regulatory Class: | Class II |
| Product Codes: | HGX |
| Indication for Use: | The Rumble Tuff Electric Breast Pump is an electrically powered |
| single-user device used to express and collect milk from the breasts | |
| of lactating women. The device is not intended for hospital use. | |
| Predicate Device(s): | Swing Breastpump (K053052) By Medela, Inc. and Lansinoh |
| Affinity Double Electric Breast Pump (DEBP) (K092783) By | |
| ENKO Ltd. | |
| 1 of 5 |
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Acute Ideas Co., Ltd 3F, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan TEL: 886-2-8751 4868 FAX: 886-2-8751 5868
The Rumble Tuff Electric Breast Pump is a powered Breast Device Description: Pump. With different models, the Pumping can be performed on one breast or on both breasts at the same time; the Rumble Tuff Electric Breast Pump can be powered by 4 AA batteries, one 7.4V Li batteries or an AC Adapter provided with the pump. The pumping system consists of a diaphragm-type vacuum pump which is driven by a microcontroller controlled DC electric motor. Rumble Tuff Electric Breast Pump has five models; PA200S, PA201S, PA201D, PA203S, and PA203D. The suffix "S" stands for the model with single collection kit, and "D" stands for the model with dual collection kits. The user interface of PA200S uses 4 LEDs for indicating pumping cycle and uses a roller type adjuster for pumping level adjustment and indicating pumping level. Models PA201S, PA201D, PA203S, and PA203D all use the same user interface, a LCD screen for showing the pumping information; it also uses a roller type adjuster for pumping level adjustment. For all models, the user is able to control the cycle speed and vacuum level. The summary of the 5 models are as follows:
| Model | PA200S | PA201S | PA203S |
|---|---|---|---|
| Pumping Suction | 125 - 250 mmHg | 115 - 250 mmHg | 115 - 250 mmHg |
| Suction Settings | 7 Levels | a) Stimulation (8 Levels)b) Expression (8 Levels) | a) Stimulation (8 Levels)b) Expression (8 Levels) |
| Power Supply | a) 4 AA Alkaline Batteriesb) 12V AC/DC Adapter | a) 7.4V Li-ion Batteryb) 12V AC/DC Adapter | a) 4 AA Alkaline Batteriesb) 12V AC/DC Adapter |
| Pumping Option | Single | Single | Single |
| Back Flow Protection | Yes | Yes | Yes |
| Interface (display) | LED indicators | LCD Screen | LCD Screen |
| Pumping Cycles | up to 1.67/sec | Up to 1.83/sec | Up to 1.11/sec |
Single Pumping Models
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Acute Ideas Co., Ltd
3F, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan TEL: 886-2-8751 4868 FAX: 886-2-8751 58
| Model | PA201D | PA203D |
|---|---|---|
| Pumping Suction | 85 – 250 mmHg | 85 – 250 mmHg |
| Suction Settings | a) Stimulation (8 levels) | a) Stimulation (8 levels) |
| b) Expression (8 levels) | b) Expression (8 levels) | |
| Power Supply | a) 7.4V Li-Ion Battery | a) 4 AA Alkaline Batteries |
| b) 12V AC/DC Adapter | b) 12V AC/DC Adapter | |
| Pumping Option | Single or Double | Single or Double |
| Back Flow Protection | Yes | Yes |
| Interface (display) | LCD Screen | LCD Screen |
| Pumping Cycles | Up to 1.23/sec | Up to 1.23/sec |
Double Pumping Models
The patient-contacting portions of the Rumble Tuff Electric Breast Materials Used: Pump are composed of polypropylene and silicone. The patientcontacting portions of the predicate devices also included polypropylene. The polypropylene and silicone in the Rumble Tuff were evaluated for biocompatibility per ISO 10993 (see testing description in the "Testing" section) and deemed biocompatible. Testing: The Rumble Tuff Electric Breast Pump is tested to meet: . IEC 60601-1:2005, "Medical Electrical Equipment, General Requirements for Safety" ● IEC 60601-1-2:2007, "Medical electrical equipment. General requirements for basic safety and essential performance. Collateral standard. Electromagnetic compatibility. " ● ISO 10993-5: 2009, "In Vitro Cytotoxicity Test of Expression collection Kit"
- ISO 10993-10: 2010, "Skin Sensitization Test of Expression collection Kit (polar and non-polar)"
- ISO 10993-10: 2010, "Skin irritation Test of Expression collection Kit {polar and non-polar}"
- Additionally, the tests of vacuum levels and cycle speeds conducted by Acute Ideas are provided to demonstrate the performance of Rumble Tuff Electric Breast Pump.
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TEL: 886-2-8751 4868 FAX: 886-2-8751 5868
Comparison to Predicate Devices:
The following table summarizes the basic similarities and differences between Rumble Tuff Electric Breast Pump and predicate devices.
For single pumping models:
| New Device | New Device | New Device | Predicate Device | |
|---|---|---|---|---|
| Device Name | Rumble Tuff ElectricBreast Pump -PA200S | Rumble Tuff ElectricBreast Pump -PA2015 | Rumble Tuff ElectricBreast Pump -PA203S | Medela Swing |
| 510(k) # | K113315 | K113315 | K113315 | K053052 |
| Product Code | HGX | HGX | HGX | HGX |
| Classification | 2 | 2 | 2 | 2 |
| Intended use | to express milk | to express milk | to express milk | to express milk |
| Power Source | a) 4 AA alkalinebatteriesb) 12V AC/DCAdapter | a) 7.4V Li-IonRechargeableBatteryb) 12V AC/DCAdapter | a) 4 AA AlkalineBatteriesb) 12V AC/DCAdapter | a) 4 AA alkalinebatteriesb) 4.8V DCAdapter |
| Pump type | Diaphragm type | Diaphragm type | Diaphragm type | Diaphragm type |
| PumpingSuction | 125 – 250 mmHg | 115 - 250 mmHg | 115 – 250 mmHg | 0 - 250 mmHg |
| Adjustablesuction level | Yes | Yes | Yes | Yes |
| Pumping Option | Single | Single | Single | Single |
| Back FlowProtection | Yes | Yes | Yes | No |
| Let DownFunction | Yes | Yes | Yes | Yes |
| Cycling /Suction ControlMechanism | Microcontroller | Microcontroller | Microcontroller | Microcontroller |
| Design ofvacuum relief | Using a vacuumrelief valve drivenby a solenoid | Using a vacuumrelief valve drivenby a solenoid | Using a vacuumrelief valve drivenby a solenoid | Using a vacuumrelief valve drivenby a solenoid |
| Material (thatmay contactuser's body) | PP for Breastshield;Silicone forBreastshield cover | PP for Breastshield;Silicone forBreastshield cover | PP for Breastshield;Silicone forBreastshield cover | PP for Breast Shield |
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Acute Ideas Co., Ltd.
3F, No.11, Lane 35, Jihu Road, Neihu Dist., Taipei, Taiwan
| New Device | New Device | Predicate Device | |
|---|---|---|---|
| Device Name | Rumble Tuff Electric BreastPump - PA201D | Rumble Tuff Electric BreastPump - PA203D | Lansinoh DEBP |
| 510(k) # | K113315 | K113315 | K092783 |
| Product Code | HGX | HGX | HGX |
| Classification | 2 | 2 | 2 |
| Intended use | to express milk | to express milk | to express milk |
| Power Source | a) 7.4V Li-IonRechargeable Batteryb) 12V AC/DC Adapter | a) 4 AA Alkaline Batteriesb) 12V AC/DC Adapter | a) 6 AA alkaline batteriesb) 9V DC Adapter |
| Pump type | Diaphragm type | Diaphragm type | Diaphragm type |
| Pumping Suction | 85 - 250 mmHg | 85 - 250 mmHg | 50 - 250 mmHg |
| Adjustablesuction level | Yes | Yes | Yes |
| Pumping Option | Single or Double | Single or Double | Single or Double |
| Back FlowProtection | Yes | Yes | Yes |
| Let DownFunction | Yes | Yes | Yes |
| Cycling/SuctionControlMechanism | Microcontroller | Microcontroller | Microcontroller |
| Design of vacuumrelief | Using a vacuum relief valvedriven by a solenoid | Using a vacuum relief valvedriven by a solenoid | Using a vacuum relief valvedriven by a solenoid |
| Material (thatmay contact user'sbody) | PP for Breastshield;Silicone for Breastshieldcover | PP for Breastshield;Silicone for Breastshieldcover | PP + TPR for Breast Shield |
For double pumping models:
Conclusion:
The Rumble Tuff Electric Breast Pumps are substantially equivalent to the predicate devices. Based upon the test data submitted, the devices provide sufficient vacuum pressure to safely and effectively express and collect milk from lactating women.
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Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002
November 20, 2012
Acute Ideas Co., Ltd. % Mr. Matthew Kho Director A Cute Baby, Inc. 865 N 1430 W OREM UT 84057
Re: K113315
Trade/Device Name: Rumble Tuff® Electric Breast Pump (Models: PA200S, PA201S, PA201D, PA203S and PA203D) Regulation Number: 21 CFR§ 884.5160 Regulation Name: Powered breast pump Regulatory Class: II Product Code: HGX Dated: November 6, 2012 Received: November 6, 2012
Dear Mr. Kho:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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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 I va must compy "Harth labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
Benjamin R. Fisher -S
Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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510(k) Number: K113315
Device Name: Rumble Tuff® Electric Breast Pump (Models: PA200S, PA201S, PA201D, PA203S and PA203D)
Indication for Use:
The Rumble Tuff Electric Breast Pump is an electrically powered single-user device to express and collect milk from the breasts of lactating women. The device is not intended for hospital use.
Prescription Use ___
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(Part 21 CFR 801 Subpart D)
(Please DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED) ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Concurrence of CDRH, Office of Device Evaluation (ODE)
Benjamin R. Fisher -S 2012.11.20 15:05:38 -05'00'
(Division Sign-Off) Division of Reproductive, Gastro-Renal, and Urological Devices K113315 510(k) Number
§ 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).