← Product Code [GEX](/submissions/SU/subpart-e%E2%80%94surgical-devices/GEX) · K140837 # LUCID LY (K140837) _Bio-Med USA, Inc. · GEX · Sep 24, 2014 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEX/K140837 ## Device Facts - **Applicant:** Bio-Med USA, Inc. - **Product Code:** [GEX](/submissions/SU/subpart-e%E2%80%94surgical-devices/GEX.md) - **Decision Date:** Sep 24, 2014 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 878.4810 - **Device Class:** Class 2 - **Review Panel:** General, Plastic Surgery - **Attributes:** Therapeutic ## Intended Use LUCID LY, the laser system is indicated for: the incision, ablation, vaporization of soft tissues for general dermatology, dermatologic and general surgical procedures for coagulation and hemostasis. 1064nm Wavelength: Tattoo removal: dark ink (black, blue and brown) Removal of Nevus of Ota Removal or lightening of unwanted hair with or without adjuvant preparation. Treatment of Common Nevi, Melasma Skin resurfacing procedures for the treatment of acne scars and wrinkle ## Device Story LUCID LY is an Nd:YAG laser system (1064nm) used in dermatology and general surgery. The device generates laser energy via a resonator and Xe-gas lamp, delivering pulses through an articulated arm and multi-spot handpiece. Physicians operate the system via an LCD touch panel and foot switch, adjusting pulse energy and spot size to optimize treatment for specific soft tissue applications. The device provides non-contact laser delivery for procedures including tattoo removal, hair removal, and skin resurfacing. By controlling energy output, the physician achieves precise tissue ablation or coagulation, benefiting patients through targeted dermatologic and surgical interventions. The system includes a closed-circuit water-to-air cooling mechanism. ## Clinical Evidence No clinical data provided. Bench testing only, including compliance with IEC 60601-1 (basic safety/performance), IEC 60601-1-2 (EMC), IEC 60601-2-22 (laser safety), and IEC 60825-1 (equipment classification). ## Technological Characteristics Nd:YAG laser system; 1064nm wavelength; 5-10ns pulse duration; 1-8mm spot size; 1.5J max energy output; Top Hat beam profile. Features 10.4" TFT LCD touch control, closed-circuit water-to-air cooling, and articulated arm delivery. Powered by 100-120VAC. Complies with IEC 60601-1, IEC 60601-1-2, IEC 60601-2-22, and IEC 60825-1. ## Regulatory 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. ## Predicate Devices - Spectra ([K113588](/device/K113588.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States of America. The seal features the department's name encircling a symbol of three stylized human profiles facing right. The profiles are stacked on top of each other, creating a sense of depth and unity. The seal is presented in black and white. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 September 24, 2014 Bio-Med USA Incorporated Mr. Young Chi President 27 New England Drive Ramsey, New Jersey 07466 Re: K140837 Trade Name: LUCID LY 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: GEX Dated: August 18, 2014 Received: August 22, 2014 Dear Mr. Chi: 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 Small Manufacturers, International and Consumer Assistance at its tollfree 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 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 yours, # David Krause -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 {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K140837 Device Name LUCID LY Indications for Use (Describe) LUCID L Y, the laser system is indicated for: the incision, ablation, vaporization of soft tissues for general dermatology, dermatologic and general surgical procedures for coagulation and hemostasis. 1064nm Wavelength: Tattoo removal: dark ink (black, blue and brown) Removal of Nevus of Ota Removal or lightening of unwanted hair with or without adjuvant preparation. Treatment of Common Nevi, Melasma Skin resurfacing procedures for the treatment of acne scars and wrinkle Type of Use (Select one or both, as applicable) 2 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) This section applies only to requirements of the Paperwork Reduction Act of 1995. # *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ # 510 (K) Summary As required by CFR 807.92(c) # 1. Manufacturer. Prepared Sept 18, 2014 BISON Medical Co., Ltd. 371-42 Gasan Dong, Geum Cheon gu. Seoul 153-803, Rep of Korea t: 822865 7121, f: 82 2 865 7131 # 2. Submitter and Contact person Bio-Med USA Inc. Young Chi, President. 27 New England Drive, Ramsey, NJ 07446. U.S.A. t: 1-973 278 5222 f: 1 201 934 6030 e mail: biomedusa@msn.com # 3. Name of Device | Trade name | : | LUCID LY | |----------------------|---|------------------------------------| | Classification name | : | Powered, Laser surgical instrument | | Common name | : | Nd:YAG Surgical Laser | | Regulation | : | 878.4810 Class II | | Classification Panel | : | General and Plastic Surgery. | | Product Code | : | GEX | # 4. Legally marketed Predicate Device | K113588 | Spectra | Nd: YAG | Lutronic Corp | |---------|---------|---------|---------------| |---------|---------|---------|---------------| Although, the predicate device has two wave length (1064nm, 532nm), and hand piece, other characteristics such as Design, Construction, Energy, Repetition rate, Cooling System, Intended use of wave length 1064nm are substantial equivalence to the proposed device. #### 5. Device Description The LUCID LY . Nd: YAG laser system produces a one pulsed beam, 1064 nm Infrared light laser oscillation in tubes; power supplies, with non-contacted mode and consists of main function, laser tube : placed in the mixed crystals of copper pipe to the heater and produces a laser beam, Resonator : amplifies the beam, through the Xe-gas contained lamp : Xe-gas contains high pressure lamp to increase specific laser beam lamp This converted light energy creates the ND:YAG crystal and exhaust from the crystal is amplified into a specific wave length. Laser energy produced is delivered to the Tissue by means of an articulated arm and a specially designed multi spot Hand Piece. {4}------------------------------------------------ The Physician can optimize the effect for different applications by controlling the energy of the laser pulse and the spot size of the treatment beam, and is able to activate laser emission using Foot Switch. ### This system also consist of Optic main Bench assembly, Fiber optic Hand pieces, LCD control panel, Cooling system. Foot Pedal Switch # 6. Performance test Clinical and Non-Clinical performance test data was not provided in this submission. But, manufactured in accordance with both mandatory and voluntary standard IEC60601-1 part 1 : General requirement for basic safety and essential performance. IEC60601-1-2: 2007 E M C test IEC60601-2-22 Part 2, Particular requirements for safety of diagnostic and Therapeutic laser IEC60825-1 :2nd ED, Equipment classification and requirement. Lucid LY, demonstrates no significant different compare to the predicate device ### 7. Intended use Lucid LY, the laser system is indicated for use to the incision, excision, ablation, vaporization of soft tissues for general dermatology, dermatologic and general surgical procedures for coagulation and hemostasis. 1064nm wave length Tattoo removal : dark ink (black, blue and brown) Removal of Nevus of Ota, Treatment of common Nevi. Melasma. Removal or lightening of unwanted hair with our without adjuvant Preparation. Skin resurfacing procedures for the treatment of acne scars and wrinkles. ### 8. Biocompatibility, Sterilization This device are non-contacted mode. Hand piece tips is made by same material as predicate device. ## 9.Conclusion. LUCID LY, Nd: YAG laser system, in this submission, is substantially equivalent to several already cleared predicate device in respect to the Intended use. Main function, Technology, Principal operation and performance. And every Safety test report show it as safe and effective as predicate device and it does not raise any additional issues for safety and effectiveness. Bio-Med Inc will update and include in this summary any other information deemed seasonally necessary by the FDA {5}------------------------------------------------ # Comparison to Predicate Device | | Proposed Device | |--------------------------|----------------------------| | Device | Lucid LY | | Manufacturer | Bison Medical Corp | | Laser type Wave | Nd:YAG | | Length Beam | 1064nm | | Profile Pulse | Top Hat Mode | | width | 5-10ns | | Fluence | up to 12 J/cm2 | | Max Energy output | 1.5j | | Max Pulse Energy | 1000mj | | Spot size | 1-8mm | | Repetition /pulse rate | 1,2,4,5,10Hz, single | | Pulse Duration Frequency | 5-10ns | | LCD | 10.4" TFT LCD touch Closed | | Cooling | circuit water to air | | Dimension (wxdxh) | 450x1040x950mm | | Input power | 100-120va / 50-60Hz | | Temperature (c') | 18-30'c | | Relative humidity | 30-75% | | Atmospheric Pressure | 700-1060hPa | | Weight Intended | 122kg | Predicate Device Spectra / K113588 Lutronic Corp # Nd:YAG 1064nm /532nm Top Hat Mode 5-10ns up to 12 j/cm2 1.5j 1200mi 1-8mm 1,2,4,5,10 Hz,signle 5-10ns 10.4"TFT LCD circuit water to air 295x656x1700mm 100-120va / 50-60Hz 18-30'c 30-75% 700-1060hPa 88kg Intended use Lucid LY : This device is intended use for the incision, excision, ablation, vaporization of soft coagulation and hemostasis, 1064nm wave length Tattoo removal : dark ink (black, blue and brown) Removal of Nevus of Ota. Treatment of common Nevi, Melasma, Removal or lightening of unwanted Hair with or without adju vant preparation, Skin resurfac ing procedures for the treatment of acne scars and wrinkle #### Spectra / K113588: Predicate Device This device is intended use for the incision, excision, ablation, vaporization of soft tissues for general dermatology, dermatologic and general surgical procedures for coagulation and hemostasis, 1064nm wave length Tattoo removal : dark ink (black, blue and brown) Removal of Nevus of Ota, Treatment of common Nevi, Melasma, Removal or lightening of unwanted hair with or without adjuvant preparation Skin resurfacing procedures for the treatment of Acne Scars and Wrinkles Lucid LY {6}------------------------------------------------ # Comparison of Treatment parameter to predicate device | Proposed device
K140837 Lucid LY | | Predicate Device
K113588 Spectra | | |------------------------------------------------------------------------------|-------------------|-------------------------------------|-----------------| | Indication for use | Spot size
(mm) | Fluence
(j/cm2) | # of Treatment | | Tattoo Removal
dark color (Black, Blue, Brown) | 3 to 5 / 3 to 4 | 6.0 to 11.0 / 6.0 to 12.0 | 2 to 5 / 2 to 5 | | Acne Scares / Wrinkle | 3 to 6 / 3 to 6 | 3.0 to 7.0 / 3.0 to 7.0 | 3 or more | | Removal or lightening
wanted hair with or without
adjuvant preparation | 6/7 | 2.0 to 3.0 / 2.5 | 1 / 1 or 2 | | Nevus of Ota | 3/3 | 5.0 to 10.0 / 6.0 to 12.0 | 4 to 8 / 4 to 8 | | Melasma | 6/8 | 1.0 to 2.0 / 1.0 to 1.5 | 6 to 8 / 8 | As like above, relate Treatment Parameter is very similar to Predicate Device, --- **Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEX/K140837](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEX/K140837) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com