(88 days)
Not Found
None
No
The summary describes a device that uses infrared energy for topical heating and does not mention any AI or ML components or functionalities.
Yes
The device is described as providing "temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain spasm, temporary increase in local circulation where applied, and the relaxation of muscle," all of which are therapeutic purposes.
No
The device is described as emitting infrared energy for topical heating, providing temporary relief for muscle and joint issues, increasing local circulation, and relaxing muscles. These are all therapeutic applications, not diagnostic ones. There is no mention of identifying, detecting, or measuring a disease or condition.
No
The intended use describes emitting energy in the infrared spectrum for topical heating, which strongly implies a hardware component is required to generate and deliver this energy. The lack of a device description prevents confirmation, but the functional description points away from a software-only device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly describes a device that applies energy to the body for therapeutic purposes (heating, pain relief, circulation increase, muscle relaxation). This is a therapeutic device, not a diagnostic one.
- IVD Definition: In Vitro Diagnostics are devices used to examine specimens (like blood, urine, tissue) taken from the human body to provide information about a person's health. This device does not involve the analysis of such specimens.
- Lack of IVD-related information: The description lacks any mention of analyzing biological samples, diagnostic purposes, or any of the typical elements associated with IVDs (like assays, reagents, or diagnostic results).
Therefore, this device falls under the category of a physical therapy or therapeutic device, not an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
Intented to use to emit energy in the infrared spectrum to provide topical heating for the purpose of temporarily elevating local tissue temperature.
Intended to use for the temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain spasm, temporary increase in local circulation where applied, and the relaxation of muscle.
Product codes
ILY
Device Description
Not Found
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Not Found
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
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.
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes forming its wing. The eagle's head is facing left, and its body is suggested by the negative space between the wing stripes. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
DEC 1 7 1999
Daniel Ye Hua President United Pacific Co., Ltd. 219 South Raymond Avenue Alhambra, CA 91801
Re: K993123
Trade Name: OK-Wide Band Spectrum Therapeutic Apparatus, Models CO1A, CO1B, CO1C, CO1D, CO2A and CO2B Regulatory Class: II Product Code: ILY Dated: September 18, 1999 · Received: September 20, 1999
Dear Mr. Hua:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
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Page 2 -- Daniel Ye Hua
This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its tollfree number (800) 638-2041 or at (301) 443-6597, or at its Internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely vours.
Sincerely, yours,
Nil R.P. Ogden
James E. Dillard III
for
Acting Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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K993123 510(k) Number (if known):
QK- WIDE BAND SPECTRUM THERAPEUTIC APPARATUS Device Name:
Indications For Use:
Intented to use to emit energy in the infrared spectrum to provide topical heating for the purpose of temporarily elevating local tissue temperature.
Intended to use for the temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain spasm, temporary increase in local circulation where applied, and the relaxation of muscle.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of General Restorative Devices
Division of General Restorative Devices
510(k) Number K93123
Prescription Asse (Par 21 CFR 801.109) ્વર
- Over-The-Counter Use
mat 1-2-96)
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