(90 days)
No
The description focuses on the mechanical function of pneumatic compression and does not mention any AI/ML components or capabilities.
Yes
The device is designed to prevent deep vein thrombosis and pulmonary embolism, which are medical conditions, thereby providing a therapeutic benefit.
No
The device is designed to increase venous blood flow to help prevent deep vein thrombosis and pulmonary embolism, which is a therapeutic rather than a diagnostic function. It applies pressure to the limb and monitors pressure within its bladders; it does not analyze patient data to provide a diagnosis.
No
The device description clearly details physical components (sleeves, tubing, bladders, connectors) and their interaction with a hardware controller to deliver pneumatic pressure, indicating it is a hardware device with potentially embedded software, not a software-only device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use/Indications for Use: The device is designed to increase venous blood flow to prevent DVT and PE. This is a therapeutic and preventative function, not a diagnostic one.
- Device Description: The description details a pneumatic compression system that applies pressure to the leg. This is a physical intervention, not a test performed on biological samples to diagnose a condition.
- Lack of IVD Characteristics: There is no mention of analyzing biological samples (blood, urine, tissue, etc.), detecting specific markers, or providing diagnostic information about a patient's condition.
IVD devices are used to examine specimens derived from the human body to provide information for the diagnosis, prevention, monitoring, treatment, or alleviation of disease. This device does not fit that description.
N/A
Intended Use / Indications for Use
The Kendall SCD Compression System is designed to increase venous blood flow in the at risk patient, including bariatric and morbidly obese patients, in order to help prevent deep vein thrombosis and pulmonary embolism.
Product codes
JOW
Device Description
The proposed devices, Sequential Compression Comfort Sleeves, are the compressible limb sleeve component of a pneumatic compression system for applying pressure to a patient's leg for the prevention of deep vein thrombosis (DVT) and pulmonary embolism (PE).
Sequential Compression Comfort Sleeves are compatible with the SCD Express Controller (K040511), SCD Response Controller (K992079) and SCD Sequel Controller (K942664), collectively referred to as SCD Controllers. SCD Controllers provide air to the sleeves through tubing connected to each bladder of the sleeve delivering an intermittent, sequentially gradient pneumatic pressure to the limb. The controller system monitors the pressure in the bladders and releases the pressure by venting the air from the sleeve bladders through a valve system within the controllers.
The proposed single-patient-use, disposable sleeves are available in knee, thigh and thigh Tear-Away styles. The Tear-Away function allows the clinician to convert the patient from a thigh length sleeve to a knee length sleeve without changing to a new sleeve. TThe sleeve connects to a controller via a 3-lumen tubing set. The tubing set connects to the sleeve via a low-profile connector that can be disengaged to allow for patient ambulation without sleeve removal.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
leg, limb
Indicated Patient Age Range
Not Found
Intended User / Care Setting
healthcare professionals
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
Product verification and validation testing as detailed in this 510(k) submission was used to demonstrate equivalence of the proposed device. Such testing included basic functional and performance tests, along with hemodynamic testing on healthy human subjects.
Intermittent pneumatic compression systems (IPC), such as the Kendall SCD Compression System, have been used clinically by healthcare professionals for over twenty years. A review of published and unpublished clinical literature identifies no major risks associated with these devices. Extensive published clinical experience with these devices confirms an acceptable risk/benefit ratio and provides substantial clinical evidence to support the following conclusions:
- Sufficient clinical literature and data exist to demonstrate the safety and performance of IPC devices.
- The objectives of the clinical review were met by an analysis of all relevant aspects of safety and performance reported in scientific literature and no gaps of information are present.
- All of the published reports examined for the clinical review are from recognized scientific, peer-reviewed journals and address the indications of the devices.
- The literature reveals little variation in the clinical indications for the use of the devices under review.
- The literature and the narrative review provide critical evaluation of the hazards and risks and appropriate safety measures for the devices with respect to patients, medical staff, and third parties.
- The patient/study populations reported in the literature, the medical purpose, indications for use, and types of diseases reported are those intended for the devices.
- The literature reviewed addresses the technology, critical performance, design, current state of the art and principles of use and features of the devices as well as competing products and technology.
- No references are identified which indicate the presence of risks inherent to the design.
- The claims made in the device labelling are substantiated by the published clinical data.
Key Metrics
Not Found
Predicate Device(s)
SCD Express System Sleeves (K040511), SCD Express Tear-Away Sleeves (K040649), SCD Large/X-Large Knee and Thigh Sleeves (K051805)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 870.5800 Compressible limb sleeve.
(a)
Identification. A compressible limb sleeve is a device that is used to prevent pooling of blood in a limb by inflating periodically a sleeve around the limb.(b)
Classification. Class II (performance standards).
0
510(k) Summary
In accordance with section 513(I) of the SMDA and as defined in 21 CFR Part 807.3 final rule dated December 14, 1994, this summary is submitted by:
Kendall, a Division of Tyco Healthcare 15 Hampshire Street Mansfield, MA 02048 Date Prepared: 29 January 2010
MAY - 4 2010
Contact Person 1.
Mia Proli Manager, Regulatory Affairs (508) 261-8037
2. Name of Medical Device
Classification Name: Sleeve, Limb, Compressible Kendall SCD™ Sequential Compression Comfort Sleeves Proprietary Name:
3. Identification of Legally Marketed Device
The proposed devices, Sequential Comfort Sleeves, are identical in intended use, function and mode of operation to the SCD Express System Sleeves (K040511); SCD Express Tear-Away Sleeves (K040649) and SCD Large/X-Large Knee and Thigh Sleeves (K051805).
4. Device Description
The proposed devices, Sequential Compression Comfort Sleeves, are the compressible limb sleeve component of a pneumatic compression system for applying pressure to a patient's leg for the prevention of deep vein thrombosis (DVT) and pulmonary embolism (PE).
Sequential Compression Comfort Sleeves are compatible with the SCD Express Controller (K040511), SCD Response Controller (K992079) and SCD Sequel Controller (K942664), collectively referred to as SCD Controllers. SCD Controllers provide air to the sleeves through tubing connected to each bladder of the sleeve delivering an intermittent, sequentially gradient pneumatic pressure to the limb. The controller system monitors the pressure in the bladders and releases the pressure by venting the air from the sleeve bladders through a valve system within the controllers.
The proposed single-patient-use, disposable sleeves are available in knee, thigh and thigh Tear-Away styles. The Tear-Away function allows the clinician to convert the patient from a thigh length sleeve to a knee length sleeve without changing to a new sleeve. TThe sleeve connects to a controller via a 3-lumen tubing set. The tubing set connects to the sleeve via a low-profile connector that can be disengaged to allow for patient ambulation without sleeve removal.
1
K100306: Kendall SCD Sequential Compression Comfort Sleeves
ട. Device Intended Use
The Kendall SCD Compression System is designed to increase venous blood flow in the at risk patient, including bariatric and morbidly obese patients, in order to help prevent deep vein thrombosis and pulmonary embolism.
6. Product Comparison
The proposed devices, Sequential Comfort Sleeves, are identical in intended use, function and mode of operation to the SCD Express System Sleeves (K040511): SCD Express Tear-Away Sleeves (K040649) and SCD Large/X-Large Knee and Thigh Sleeves (K051805).
The predicate SCD Sleeves are constructed of two layers of non-woven polyester laminated to a thin film of PVC that are welded together to form bladders. Tubes are attached to the bladders via rigid PVC inlet ports which are welded to the laminate material. To make the sleeves more comfortable, the proposed Comfort Sleeves will be constructed of four layers; two lavers of non-laminated PVC welded together to form bladders with covers made from both a polyester mesh fabric and a wickable polyester fabric, which form a "pillowcase" around the bladders. In this design, the tubing will be welded into the bladders, beneath the sleeves, without the use of an inlet port.
7. Product Testing
There are no FDA performance standards established and required for the proposed device. However, the standards listed in the table below have been reviewed and applied in whole or in part as deemed appropriate during design, development, and manufacture of the proposed device:
| Standard
| Number | Standard Title | Version |
|---|---|---|
| ISO 10993-1 | Biological Evaluation of Medical Devices Part 1: Evaluation and | |
| Testing | 2003 | |
| ISTA 2A | ISTA Preshipment Testing Procedures - Combination Tests for | |
| Packaged Products | 2008 |
Product verification and validation testing as detailed in this 510(k) submission was used to demonstrate equivalence of the proposed device. Such testing included basic functional and performance tests, along with hemodynamic testing on healthy human subjects.
Intermittent pneumatic compression systems (IPC), such as the Kendall SCD Compression System, have been used clinically by healthcare professionals for over twenty years. A review of published and unpublished clinical literature identifies no major risks associated with these devices. Extensive published clinical experience with these devices confirms an acceptable risk/benefit ratio and provides substantial clinical evidence to support the following conclusions:
-
- Sufficient clinical literature and data exist to demonstrate the safety and performance of IPC devices.
-
- The objectives of the clinical review were met by an analysis of all relevant aspects of safety and performance reported in scientific literature and no gaps of information are present.
-
- All of the published reports examined for the clinical review are from recognized scientific, peer-reviewed journals and address the indications of the devices.
ﺘ
2
K100306: Kendall SCD Sequential Compression Comfort Sleeves
- The literature reveals little variation in the clinical indications for the use of the devices 4. under review.
-
- The literature and the narrative review provide critical evaluation of the hazards and risks and appropriate safety measures for the devices with respect to patients, medical staff, and third parties.
-
- The patient/study populations reported in the literature, the medical purpose, indications for use, and types of diseases reported are those intended for the devices.
-
- The literature reviewed addresses the technology, critical performance, design, current state of the art and principles of use and features of the devices as well as competing products and technology.
-
- No references are identified which indicate the presence of risks inherent to the design.
-
- The claims made in the device labelling are substantiated by the published clinical data.
8. Conclusion
・
Product verification and validation testing and a review of clinical literature demonstrate that Kendall Sequential Compression Comfort Sleeves are as safe, as effective and perform as well as the predicate devices.
Sequential Compression Comfort Sleeves are substantially equivalent to the predicate devices in the following areas:
- Both the proposed and predicate devices are intended to be used with the SCD Express . Controller (K040511), SCD Response Controller (K992079) and SCD Sequel Controller (K942664).
- When connected to a compression system, both the proposed and predicated devices . are compressible limb sleeves designed to increase blood flow by applying pressure to a patient's limb for the prevention of deep vein thrombosis and pulmonary embolism.
3
Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular arrangement of text reading "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA". Inside the circle is a stylized image of an eagle or bird with three human profiles incorporated into its design. The bird's head and neck are formed by the silhouettes of three faces, suggesting a connection between health, humanity, and government services.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room W-O66-0609 Silver Spring, MD 20993-0002
Covidien c/o Mia Proli Manager, Regulatory Affairs 15 Hampshire Street Mansfield, MA 02048
MAY - 4 2010
Re: K100306
Kendall SCDTM Sequential Compression Comfort Sleeves Regulation Number: 21 CFR 870.5800 Regulation Name: Compressible Limb Sleeve Regulatory Class: Class II (two) Product Code: JOW Dated: January 29, 2010 Received: February 3, 2010
Dear Ms. Proli:
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.
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
4
Page 2 - Ms. Mia Proli
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 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.html 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 vours.
Dina R. Vihmer
Bram D. Zuckerman, M.D.
Director
Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
Indications for Use Statement
510(k) Number (if known): K100306
Device Name: Sequential Compression Comfort Sleeves
Indications for Use: The Kendall SCD Compression System is designed to increase venous blood flow in at risk patients, including bariatric and morbidly obese patients, in order to help prevent deep vein thrombosis and pulmonary embolism.
Prescription Use _ X
OR ·
Over-The-Counter Use (Per 21 CFR 801.109)
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Concurrence of CDRH, Office of Device Evaluation (ODE)
Dma R. V. Lumer
(Division Sign-Off) (Division Sign Sign Sin, Devices
510(k) Number صكصلاحصاليك ك