(260 days)
Not Found
No
The device description and performance studies focus on the physical design, light emission, and electrical performance, with no mention of AI or ML.
Yes
The device is intended for the "treatment of full face wrinkles," which is a therapeutic claim.
No
The device is intended for the treatment of full face wrinkles and does not gather or analyze data to diagnose a condition.
No
The device description clearly outlines a physical, handheld device made of ABS plastic and stainless steel, emitting LED light. This indicates a hardware component is central to its function, not just software.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is "for in the treatment of full face wrinkles." This describes a therapeutic or cosmetic treatment applied directly to the body, not a test performed on a sample taken from the body to diagnose a condition.
- Device Description: The description details a light-emitting device used for treatment, not a device designed to analyze biological samples.
- Lack of IVD Characteristics: The description does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples (blood, urine, tissue, etc.)
- Detecting or measuring substances in samples
- Providing information for diagnosis, monitoring, or screening of diseases or conditions
Based on the provided information, the SL-8813 is a light therapy device intended for cosmetic treatment of wrinkles.
N/A
Intended Use / Indications for Use
SL-8813 is an Over The Counter (OTC) handheld device intended for in the treatment of full face wrinkles.
The SL8813 is an Over The Counter (OTC) handheld device intended for use in the treatment of full face wrinkles.
Product codes (comma separated list FDA assigned to the subject device)
OHS
Device Description
SL-8813 is a handheld ergonomically designed ABS plastic housed device with a locking Medical Grade Stainless Steel retainer holding in place a Medical Grade USP Class polycarbonate lens from which high spectral purity LED light in 4 (four) specific wavelengths is emitted. By design the optical output has a high degree of homogenous light distribution. The output wavelengths are actuated via a simple on-off swipe button and are in the visible Red and the Infrared spectrum. SL8813 is powered by a built in (non user accessible) Lithium lon Battery which can be charged as required via a supplied UL listed AC/DC wall mounted unit. Treatment time for light outputs is controlled by the operator as per Treatment Protocols listed in User Documentation. Audible announcement is provided to the user for timing intervals of treatments and is so noted in User Documentation.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Full face
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Over The Counter patient usage
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)
Evaluation Testing:
- SL-8813 electro-optical performance verification of LED power densities (mW/Cm2), pattern homogenous-ness and electrical performance were conducted referencing Table 1 International Standards.
- Safety and essential performance designed for and validated referencing Table 1 International Standards.
- SL-8813 optical energy output fluences are set in each specific wavelength to minimally meet the claimed fluence levels in each of the specific wavelengths as the Primary Predicate devices
Clinical Testing:
There were no clinical test requirements for this submission. An addendum Usability / Self Selection study was performed.
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.
K120775, K120560, K130225, K092460
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
§ 878.4810 Laser surgical instrument for use in general and plastic surgery and in dermatology.
(a)
Identification. (1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
(b)
Classification. (1) Class II.(2) Class I for special laser gas mixtures used as a lasing medium for this class of lasers. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 878.9.
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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 representation of three human profiles facing right, arranged in a way that suggests unity and connection. The profiles are black and are set against a white background. Encircling the profiles are the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
August 6, 2014
PS Advanced Engineering CD Feak President 200 South Garfield Avenue, Suite 103 Alhambra, California 91801
Re: K133546 Trade/Device Name: StarLite-OM SL-8813 Regulation Number: 21 CFR 878.4810 Regulation Name: Laser surgical instrument for use in general and plastic surgery and in dermatology Regulatory Class: Class II Product Code: OHS Dated: June 30, 2014 Received: June 30, 2014
Dear Feak:
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 (reporting of medical
1
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 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/Resourcesfor You/Industry/default.htm. 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 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 yours,
David Krause -S
- Binita S. Ashar, M.D., M.B.A., F.A.C.S. for 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) K133546
Device Name StarLite-OM SL-8813
Indications for Use (Describe)
SL-8813 is an Over The Counter (OTC) handheld device intended for in the treatment of full face wrinkles
Type of Use (Select one or both, as applicable)
- Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.
FOR FDA USE ONLY
Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)
Neil R Ogden -S 2014.08.04 15:17:58 -04'00
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DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
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Image /page/3/Picture/0 description: The image shows the logo for PS Advanced Engineering. The logo features two palm trees on the left side. To the right of the trees, the text "PS ADVANCED ENGINEERING" is written in a stylized font. Below the company name, the text "Alhambra, California, USA" is written in a smaller font.
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510(k) Summary
This 510(k) Summary of Safety and Effectiveness is being submitted in accordance with the requirements of 21 CFR 807.92
1) General Information
| Submitter: | PS Advanced Engineering
200 South Garfield Ave
Suite 103
Alhambra, Calif.
91801 |
| ------------ | --------------------------------------------------------------------------------------------- |
|---|
-
C D Feak Contact Person: President PS Advanced Engineering 200 South Garfield Ave Suite 103 Alhambra, Calif. 91801
Summary Preparation Date: 24 October 2013 -
- Product Code = OHS
-
- Product Names :
| Device Common Name: | Light Based Over The Counter Wrinkle Reduction |
|---|---|
| Device Model Number : | SL88-13 |
| Trade Names: | StarLite-OM, Light Effects, Thibiant |
| Classification Name: | Laser Instrument, Surgical Powered - General and Plastic Surgery – Class II, Gen 79-GEX |
Although this device is not a Laser and is intended for Over The Counter use, the manufacturer believes this is the classification name which is most applicable and is the same classification as the LightStim (K120775), Trinity Wrinkle Reducer (K120560), Baby Quasar Plus (K130225) and StarLite-LM (K092460) devices.
Indications for Use: The SL8813 is an Over The Counter (OTC) handheld device intended for use in the treatment of full face wrinkles.
4
4) Predicate Devices
Primary: LightStim for Wrinkles (K120775), Trinity Wrinkle Reducer (K120560), Baby Quasar Plus (K130225) Secondary: StarLite-LM (K092460)
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Summary Descriptive Sections:
5) Device Description
SL-8813 is a handheld ergonomically designed ABS plastic housed device with a locking Medical Grade Stainless Steel retainer holding in place a Medical Grade USP Class polycarbonate lens from which high spectral purity LED light in 4 (four) specific wavelengths is emitted. By design the optical output has a high degree of homogenous light distribution. The output wavelengths are actuated via a simple on-off swipe button and are in the visible Red and the Infrared spectrum. SL8813 is powered by a built in (non user accessible) Lithium lon Battery which can be charged as required via a supplied UL listed AC/DC wall mounted unit. Treatment time for light outputs is controlled by the operator as per Treatment Protocols listed in User Documentation. Audible announcement is provided to the user for timing intervals of treatments and is so noted in User Documentation.
6) Substantial equivalence in Indications for Use
The SL-8813 and the Predicate devices are hand held LED emitting devices intended for Over The Counter patient usage to specifically reduce facial wrinkles.
The target patient population for SL-8813 is identical to the population of the predicate devices.
SL-8813 and the Primary Predicate devices claim to emit identical frequencies or wavelengths of LED light energy with all claiming to meet 65mW/cm2 fluence levels with specific irradiance level distributions for the wavelengths and using the same treatment methods for the same treatment areas.
All devices emit in the Red and Infrared region within the "human safe" EC 62471 AND EU DIRECTIVE 2006/25/EC classification.
7) Performance Data compliant to Predicate Devices
- a) Evaluation Testing:
-
- SL-8813 electro-optical performance verification of LED power densities (mW/Cm2), pattern homogenous-ness and electrical performance were conducted referencing Table 1 International Standards.
-
- Safety and essential performance designed for and validated referencing Table 1 International Standards.
-
- SL-8813 optical energy output fluences are set in each specific wavelength to minimally meet the claimed fluence levels in each of the specific wavelengths as the Primary Predicate devices
-
Based on analysis of the performance, indications for user demographic base, safety and effectiveness characteristics for SL-8813, PS Advanced Engineering (PSAE) believes that the SL-8813 meets all criteria claimed by the previously approved Primary Predicate Devices.
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8) Performance Data compliant to Secondary K092460
Based on an identical physical design and fitment as well as a simpler variation of the same methods of user operation and very close to identical wording and packaging design and an identical user demographic base, PSAE believes that no significant differences in those specific characteristics exists between the SL-8813 and the previously approved StarLite-LM device (K092460).
Therefore SL-8813 raises no new questions of safety, and an addendum Usability Study was performed to evaluate Self Selection and other considerations for Human Factors - Usability comprehension to assess differences in packaging design and modified indications for use between the SL-8813 and the Secondary Predicate .
9) Table 1 - Applied International Standards
| ANSI/AAMI ES60601-1:2005/(R)2012 and
A1:2012, C1:2009/(R)2012 and
A2:2010/(R)2012 (Consolidated Text) | Medical Electrical Equipment - Part 1:
General Requirements for Basic Safety
and Essential Performance (IEC 60601-
1:2005, MOD) |
|-------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| IEC 61000-4-3 Ed 3.0 2006-02 | Electro Magnetic Compatibility - Testing
and measurement techniques - Radiated,
radio frequency, electromagnetic field
immunity test |
| CEI/IEC 62304:2006 Ed1 2006-05 | Medical Device Software - Software life
cycle processes |
| IEC 61000-4-2 Ed 2.0 2008-12 | Electromagnetic Compatibility (EMC)
Testing and measurement techniques -
Electrostatic discharge immunity test |
| ANSI/AAMI IEC 60601-2:2007(R) 2012 | Medical Electrical Equipment - Part 1-2:
General requirements for basic safety and
essential performance - Collateral
Standard: Electromagnetic compatibility -
Requirements and Tests |
| EN ISO 14791:2012 | Medical Devices - Application of risk
management to Medical Devices |
| IEC/TR 62471-2 Ed 1.0 2009-08 | Photobiological safety of lamps and lamp
systems - Part 2 Guidance on
manufacturing requirements relating
to
non-laser optical radiation safety |
10) Clinical Testing
There were no clinical test requirements for this submission. An addendum Usability / Self Selection study was performed.
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