(17 days)
Not Found
No
The description focuses on hardware components and basic heat therapy, with no mention of AI/ML terms or functionalities.
Yes
The device description explicitly states it is a "therapeutic medical device."
No
The device is described as a "therapeutic medical device" intended for pain relief and increased blood circulation through heat therapy, not for diagnosing conditions.
No
The device description explicitly states it is an "AC operated, non-invasive, therapeutic medical device" consisting of a "Control Unit" and "treatment probes" containing "infrared and visible laser diodes," indicating it is a hardware-based device.
Based on the provided information, the Luminex Infrared Lamp System is not an IVD (In Vitro Diagnostic) device.
Here's why:
- Intended Use: The intended use clearly states that the device is for providing topical heating to the body for therapeutic purposes (pain relief, increased circulation, muscle relaxation). This is a direct interaction with the patient's body.
- Device Description: The description confirms it's a non-invasive, therapeutic medical device that applies heat directly to the skin.
- Lack of IVD Characteristics: IVD devices are used to examine specimens (like blood, urine, tissue) outside of the body to provide information about a person's health. The Luminex system does not involve any specimen collection or analysis.
Therefore, the Luminex Infrared Lamp System falls under the category of a therapeutic medical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The Luminex Infrared Lamp System is intended to emit energy in the visible and near infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and/or the temporary relaxation of muscle.
Product codes
ILY
Device Description
The Luminex Infrared Lamp System is an AC operated, non-invasive, therapeutic medical device that provides continuous heat therapy through the use of infrared and visible laser diodes. The system consists of a Control Unit that houses the electronics and controls, and treatment probes that contain the infrared and visible laser diodes. The probes are intended to be placed directly on the skin to provide topical heating.
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
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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)
Testing of the Luminex Infrared Lamp System includes functional performance testing and electrical safety testing in accordance with all applicable standards for Infrared Lamp Systems of this type.
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
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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f082969
APPENDIX C
OCT 2 3 2008
SUMMARY OF SAFETY AND EFFICACY
(Per 21 CFR Part 807.92)
I. GENERAL INFORMATION
| Device Generic Name: | Infrared Lamp |
|---|---|
| Trade Name: | Luminex Infrared Lamp System |
| Device Classification: | Class II, Performance Standards |
| 21CFR Part 890.5500 - Lamp, Infrared, | |
| Therapeutic Heating | |
| Product Code: | ILY |
| Applicant Name and Address: | Medical Laser Systems, Inc. |
| 20 Baldwin Drive | |
| Branford, CT 60405 | |
| 203 / 481-2395 | |
| Brian D. Richardson, President | |
| Key Contact: | Miki Kolton, Regulatory Consultant |
| Greenberq, Traurig, LLP | |
| 800 Connecticut Ave NW Suite 500 | |
| Washington, DC 20006 | |
| 202-331-3100 | |
| 510(k) Number: | Pending |
II. DEVICE DESCRIPTION
The Luminex Infrared Lamp System is an AC operated, non-invasive, therapeutic medical device that provides continuous heat therapy through the use of infrared and visible laser diodes. The system consists of a Control Unit that houses the electronics and controls, and treatment probes that contain the infrared and visible laser diodes. The probes are intended to be placed directly on the skin to provide topical heating.
III. INDICATIONS FOR USE
The Luminex Infrared Lamp System is intended to emit energy in the visible and near infrared spectrum to provide topical heating for the purpose of elevating
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tissue temperature for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and/or the temporary relaxation of muscle.
IV. Predicate Devices
Predicate devices to the Luminex Infrared Lamp System include, but are not limited to, the Thor DDII IR Lamp System (K033923), the Maestro MDTL Laser System (K053473), and the Vectra Genisys Laser System (K040662).
V. Summary of the Technical Characteristics of the Luminex System as Related to the Referenced Predicate Devices.
The Luminex Infrared Lamp System and the aforementioned predicate devices are infrared lamps as defined in 21 CFR 890.5500. These devices utilize infrared and visible diodes to generate topical heating for the purpose of elevating tissue temperatures for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm, the temporary increase in local circulation and the temporary relaxation of muscle. The Luminex Infrared Lamp System and the aforementioned predicate devices have the same intended uses and similar technical and performance characteristics.
VI. Testing
Testing of the Luminex Infrared Lamp System includes functional performance testing and electrical safety testing in accordance with all applicable standards for Infrared Lamp Systems of this type.
VII. Conclusions
Pursuant to the testing and comparison to the predicate devices, the Luminex Infrared Lamp System has the equivalent intended uses, with similar technical and performance characteristics. The Luminex Infrared Lamp System complies with the generally accepted therapeutic heat performance specifications by producing a level of tissue temperature reported in the literature and accepted by the Federal Food and Druq Administration.
The Luminex Infrared Lamp System performs as intended and does not raise any new safety or efficacy issues.
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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with its wings spread, and the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the eagle. The eagle is black, and the text is also black. The logo is simple and recognizable.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 2 3 2008
Medical Laser Systems, Inc. % Greenberg, Traurig, LLP Ms. Miki Kolton 800 Connecticut Avenue NW. Suite 500 Washington, District of Columbia 20006
Re: K082969
Trade/Device Name: Luminex Infrared Lamp System Regulation Number: 21 CFR 890.5500 Regulation Name: Infrared lamp Regulatory Class: II Product Code: ILY Dated: September 22, 2008 Received: October 8, 2008
Dear Ms. Kolton:
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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), 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 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); 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.
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Page 2 - Ms. Miki Kolton
This letter will allow you to begin marketing your device as described in your Section 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), please contact the Center for Devices and Radiological Health's (CDRH's) Office of Compliance at (240) 276-0115. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Protmarket, Surveillance at (240) 276-3474. For questions regarding the reporting of device adverse events, (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at (240) 276-3464. 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours.
Mark M. Mikkelson
Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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APPENDIX A
Indications for Use Statement
510(k) Number (if known):
Pending
Device Name:
Luminex Infrared Lamp System
Indications for Use:
The Luminex Infrared Lamp System is intended to emit energy in the visible and near infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and/or the temporary relaxation of muscle.
Prescription Use: X AND/OR Over the Counter Use: (Part 21 CFR 801 Subpart D) (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODpE)
Nitrogen for men
(Division Sign-Off)" Division of General, Restorative, and Neurological Devices
510(k) Number K082969