(116 days)
Not Found
No
The description focuses on hardware components, safety mechanisms, and basic software control for light emission and temperature monitoring. There is no mention of AI, ML, or any learning/adaptive capabilities.
Yes
The "Intended Use / Indications for Use" section explicitly states that the device provides "temporary relief/reduction of minor muscular and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local blood circulation, and temporary relaxation of muscles," which are therapeutic effects. Additionally, the "Device Description" characterizes it as a "therapeutic device."
No
Explanation: The device is described as a "therapeutic device" intended to provide topical heating for temporary relief of pain and stiffness, increase blood circulation, and relax muscles. It facilitates treatment, not diagnosis.
No
The device description clearly outlines hardware components such as semiconductor laser diodes, a flexible pad, a battery pack, electrical cables, a microprocessor, fans, capacitive proximity sensors, body temperature sensors, an ambient light sensor, and reference voltage monitoring systems. While it mentions being "software controlled," it is fundamentally a hardware device that utilizes software for control and monitoring.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is for "topical heating for the purpose of elevating tissue temperature for the temporary relief/reduction of minor muscular and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local blood circulation, and temporary relaxation of muscles." This describes a therapeutic application on the body, not a diagnostic test performed on samples taken from the body.
- Device Description: The description details a device that emits light onto the body for therapeutic purposes. It does not mention any interaction with biological samples (like blood, urine, tissue, etc.) for the purpose of diagnosis.
- Lack of IVD Characteristics: The information does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples.
- Detecting or measuring substances in biological samples.
- Providing information for the diagnosis, monitoring, or prognosis of a disease or condition.
Therefore, the Softcure TM 96 is a therapeutic device, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
The Softcure TM 96 is intended to emit energy in the visible spectrum (red 635mm) to provide topical heating for the purpose of elevating tissue temperature for the temporary relief/reduction of minor muscular and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local blood circulation, and temporary relaxation of muscles.
Product codes (comma separated list FDA assigned to the subject device)
ILY
Device Description
The Wellray® Medical Laser Softcure™ 96 is a therapeutic device using wavelengths of monochromatic light produced by semiconductor laser diodes to treat a variety of musculoskeletal concerns. The Softcure ™ 96 is a portable and wearable, battery powered, software controlled device intended for use on the body such as the back, legs, chest, arms or other areas where therapeutic light may be beneficial. A flexible pad, drawing power through an electrical cable from a carry able battery pack, emits red (635nm) light by means of semiconductor laser diodes to the desired body area. The flexible pad is designed to conform to the contour of the treatment site providing uniform treatment dosage over nonplanar body physique. The semiconductor laser diodes are monitored for temperature and light output by a microprocessor and cooled by variable speed fans to ensure the optimum light output. The lasers are allowed to energize only when four separate failsafe monitoring systems sense that the flexible pad is brought into close contact with the user's body. These failsafe systems include capacitive proximity sensors, body temperature sensors, an ambient light sensor and reference voltage monitoring.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
back, legs, chest, arms or other areas where therapeutic light may be beneficial.
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
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)
Performance Testing Bench: Electrical safety and functional performance testing were conducted on the Softcure™ 96 demonstrating that the device is compliant with FDA 21 CFR J 1040.10 and 1040.11 standards, AAMI/ANSI ES 60601-1 Medical Electrical Equipment - Part 1: General Requirements for Safety and Essential Performance AAMI/ANSI ES 60601-1:2005/(R)2012 and A1:2012), IEC 60601-1-2 Medical Electrical Equipment -Part 1-2: General Requirements for Safety and Essential Performance - Collateral Standard: Electromagnetic Compatibility - Requirements and tests, 2007-03.
Performance Testing Non-Clinical: The Softcure™ 96 is capable of achieving therapeutic heat temperature of 40 – 45 degrees centigrade. An increase in topical heating of the tissue level by at least 5 degrees centigrade was reached within one (1) minute. The therapeutic temperature range was maintained for at least ninety (90) minutes. The temperature versus time measurements were conducted on 8 subjects at various physical locations, i.e., leg, neck, back and shoulder. The pre-exposed topical skin temperature ranged from 36 to 39 degrees centigrade. These data demonstrate that the Softcure™ 96 meets the generally accepted topical temperature range for therapeutic heat of 40-45 degrees centigrade during the recommended treatment time.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
K051816, K121920, K931261, K131113
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
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
§ 890.5500 Infrared lamp.
(a)
Identification. An infrared lamp is a device intended for medical purposes that emits energy at infrared frequencies (approximately 700 nanometers to 50,000 nanometers) to provide topical heating.(b)
Classification. Class II (special controls). The device, when it is an infrared therapeutic heating lamp, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 890.9.
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Image /page/0/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
May 5, 2017
Wellray Medical Laser, Inc. Mr. Richard DeRoberts Chief Executive Officer 216 Moores Run Rd. Wardensville, West Virginia 26851
Re: K170068
Trade/Device Name: Softcure 96 Regulation Number: 21 CFR 890.5500 Regulation Name: Infrared Lamp Regulatory Class: Class II Product Code: ILY Dated: February 8, 2017 Received: February 8, 2017
Dear Mr. DeRoberts:
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 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
1
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 contact the Division of Industry and Consumer Education 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. 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
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 Industry and Consumer Education 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.
Jennifer R. Stevenson -S
For Binita S. Ashar, M.D., M.B.A., F.A.C.S. Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K170068
Device Name Softcure TM 96
Indications for Use (Describe)
The Softcure TM 96 is intended to emit energy in the visible spectrum (red 635mm) to provide topical heating for the purpose of elevating tissue temperature for the temporary relief/reduction of minor muscular and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local blood circulation, and temporary relaxation of muscles.
| Type of Use (Select one or both, as applicable) |
|---|
| ------------------------------------------------- |
| X 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
This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21CFR 807.92.
A. Submitter: Wellray Medical Laser, Inc. 216 Moores Run Rd. Wardensville, WV 26851 USA
Phone: 304-874-4209 Fax: 304-874-4209
Contact: Mr. Richard O. DeRoberts CEO
Date prepared: January 4, 2017
B. Device Names:
Proprietary Name: Common/Usual Name: Classification Name:
Softcure™ 96 Infrared Therapeutic Heating Lamp Infrared Lamp
C. Predicate Devices Biocare™ Lumiwave® K051816 Sunetics Laser Brush, LHB 12 K121920 Anodyne® Therapy 480 Pro K931261 Biophotas Celluma ™ K131113
Device Description: D.
The Wellray® Medical Laser Softcure™ 96 is a therapeutic device using wavelengths of monochromatic light produced by semiconductor laser diodes to treat a variety of musculoskeletal concerns. The Softcure ™ 96 is a portable and wearable, battery powered, software controlled device intended for use on the body such as the back, legs, chest, arms or other areas where therapeutic light may be beneficial. A flexible pad, drawing power through an electrical cable from a carry able battery pack, emits red (635nm) light by means of semiconductor laser diodes to the desired body area. The flexible pad is designed to conform to the contour of the treatment site providing uniform treatment dosage over nonplanar body physique. The semiconductor laser diodes are monitored for temperature and light output by a microprocessor and cooled by variable speed fans to ensure the optimum light output. The lasers are allowed to energize only when four separate failsafe monitoring systems sense that the flexible pad is brought into close contact with the user's body. These failsafe systems include capacitive proximity sensors, body temperature sensors, an ambient light sensor and reference voltage monitoring.
E. Intended Use:
The Softcure™ 96 is intended to emit energy in the visible spectrum (red 635nm) to provide topical heating for the purpose of elevating tissue temperature for the temporary relief/reduction of minor muscular and joint pain and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local blood circulation, and temporary relaxation of muscles.
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ட் Substantial Equivalence:
The Softcure™ 96 is substantially equivalent to the Biocare ™ Lumiwave® K051816, the Sunetics Laser Brush, LHB 12 - K121920, the Anodyne® Therapy 480 Pro - K931261 and the Biophotas Celluma ™ - K131113 as summarized in the following table. The Softcure ™ 96 and the predicate devices have the same intended use, the same diffused light characteristic, the same software control, the same use of a treatment timer, the same over-the-counter (OTC) use, the same method of administration (topical), the same configuration (pads/pods), and the same electrical safety.
| Predicate Device | Manufacturer | 510(k) Number |
|---|---|---|
| Lumiwave® | Biocare TM | K051816 |
| Laser Brush, LHB 12 | Sunetics | K121920 |
| 480 Pro | Anodyne® Therapy | K931261 |
| Celluma TM | Biophotas | K131113 |
Where the Softcure ™ 96 differs is that it is wearable and is powered by a battery so that the user can move around the treatment site or home and perform light tasks. It also differs in that it has multiple failure detection/shut off controls and multiple failsafe monitoring systems.
The differences identified above do not impact adversely the Safety and Effectiveness of the Softcure TM 96 device.
Performance data have been included to demonstrate that the Softcure ™ 96 device meets its specifications, and functions safely.
Performance Testing Bench G.
Electrical safety and functional performance testing were conducted on the Softcure™ 96 demonstrating that the device is compliant with FDA 21 CFR J 1040.10 and 1040.11 standards, AAMI/ANSI ES 60601-1 Medical Electrical Equipment - Part 1: General Requirements for Safety and Essential Performance AAMI/ANSI ES 60601-1:2005/(R)2012 and A1:2012), IEC 60601-1-2 Medical Electrical Equipment -Part 1-2: General Requirements for Safety and Essential Performance - Collateral Standard: Electromagnetic Compatibility - Requirements and tests, 2007-03.
H. Performance Testing Non-Clinical
The use of light energy to generate heat for therapeutic use has been well documented and is a generally accepted alternative treatment modality for the temporary relief of pain and tissue repair.
The Softcure™ 96 is capable of achieving therapeutic heat temperature of 40 – 45 degrees centigrade as accepted by the FDA. An increase in topical heating of the tissue level by at least 5 degrees centigrade was reached within one (1) minute. The therapeutic temperature range was maintained for at least ninety (90) minutes.
The temperature versus time measurements were conducted on 8 subjects at various physical locations, i.e., leg, neck, back and shoulder. The pre-exposed topical skin temperature ranged from 36 to 39 degrees centigrade. These data demonstrate that the Softcure™ 96 meets the generally accepted topical
5
temperature range for therapeutic heat of 40-45 degrees centigrade during the recommended treatment time.
l. Conclusion
The Softcure ™ 96 device is substantially equivalent to the predicate devices K051816, K121920, K931261 and K131113.