← Product Code [KGO](/submissions/SU/subpart-e%E2%80%94surgical-devices/KGO) · K052030 # SURGEON'S GLOVE, POWDER FREE (K052030) _Shun Thai Rubber Gloves Industry Public Co., Ltd. · KGO · Sep 13, 2005 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K052030 ## Device Facts - **Applicant:** Shun Thai Rubber Gloves Industry Public Co., Ltd. - **Product Code:** [KGO](/submissions/SU/subpart-e%E2%80%94surgical-devices/KGO.md) - **Decision Date:** Sep 13, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 878.4460 - **Device Class:** Class 1 - **Review Panel:** General, Plastic Surgery ## Intended Use The Royal Guard Latex, Powder-Free, Surgeon's Glove - Sterile, is a device made of natural or synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination between patient and operating room personnel. ## Device Story Device is a sterile, powder-free surgeon's glove composed of natural or synthetic rubber. Used in operating room environments by surgical personnel. Primary function is to serve as a protective barrier to prevent cross-contamination between the patient's surgical wound and the healthcare provider. Device is a single-use, disposable physical barrier. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Material: Natural or synthetic rubber. Form factor: Surgeon's glove. Sterile. Powder-free. ## Regulatory Identification A non-powdered surgeon's glove is a device intended to be worn on the hands of operating room personnel to protect a surgical wound from contamination. A non-powdered surgeon's glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing. ## 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 logo for the Department of Health and Human Services (HHS). The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH AND HUMAN SERVICES . USA" arranged around the perimeter. Inside the circle is a stylized graphic of three wavy lines that resemble a human figure. SEP 1 3 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Anan Jetsadawisut Managing Director Managing Diroctor Shun Thai Rubber Gloves Industry Public Co., Ltd. 9, Moo 4, Kached Muang, Rayong 21110 THAILAND Re: K052030 K052050 Trade/Device Name: Surgeon's Glove Powder Free Regulation Number: 21 CFR 878.4460 Regulation Name: Surgeon's Glove Regulatory Class: I Product Code: KGO Dated: September 7, 2005 Received: September 9, 2005 Dear Mr. Jetsadawisut: We have reviewed your Section 510(k) premarket notification of intent to market the device We have reviewed your Section - Forty premained in substantially equivalent (for the indications referenced above and have decembined the devices marketed in interstate for use stated in the enclosure) to legally marketed predicate devices Amendments for use stated in the encrosure for legally manced promotical Device Amendments, or to commerce prior to May 28, 1976, the enactment date of the Federal Food. Drug commerce prior to May 28, 1970, the charge with the provisions of the Federal Food, Drug, devices that have been recuire approval of a premarket approval application (PMA). and Cosmetic Act (Act) that do not require approval of a provisions of the Act. The and Cosmetic Act (Act) that do not require upproval of the general controls provisions of the Act. The Act. The You may, therefore, market the device, but in gents for annual registration, listing of general controls provisions of the Act include requirements for answereding and general controls provisions of the Fret mercial requirement misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it If your device is classified (See above) mo chairs are regulations affecting your device can may be subject to such additional controls. Existing major regulation EDA may may be subject to such adultional controlls. Extrems and to 898. In addition, FDA may be found in the Code of Federal Regulations, Title 21, Parts 800 Register be found in the Code of Federal Regarations, would be in the Federal Register. {1}------------------------------------------------ #### Page 2 - Mr. Jetsadawisut Please be advised that FDA's issuance of a substantial equivalence determination does not mean Please be advised that FDA s issualice of a subsmither requirements of the Act that FDA has made a determination that your device of an Fareseas. You must that FDA has made a determination and your areas by other Federal agencies. You must or any Federal statutes and regulations administered by registration and listin or any Federal statules and regulations administed to: registration and listing (21 l comply with all the Act's requirements, including, but not reasurements as set comply with all the Act S requirements, mendably on and ice requirements as set CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice the electronic CFR Part 807); labeling (21 CFR Part 800); and if applicable, the electronic forth in the quality systems (QS) regulation (21 CFR Patt 820); and if applicable, the electronic forth in the quality systems (Q5) regulation (Sections 531-542 of the Acction S product radiation control provisions (occions of the saces )) This letter will allow you to begin marketing your device of your device to a legal This letter will allow you to begin makemig your aftire as walevice of your device to a legally premarket notification. The FDA finding of substantial equipe and this permit premarket notification. The FDA inding of substantial equivalence 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 r the results of the may and 15 at the colors note the regulation entitled If you desire specific advice for your de not on S. Also, please note the regulation entitled, contact the Office of Complance at (246) 276 - 6178 (21CFR Part 807.97). You may obtain "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may ob "Misbranding by reference to prehance notifieddender the Act from the Division of Small other general information on your responsibilities under the Act from worker (800) 638 other general information on your responsion its toll-free number (800) 638-2041 or Manufacturers, International and Consumer Assistance at its toll-fired status and Manufacturers, International and Consumer Association of and consisted on the manufactures html. Sincerely yours, Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## INDICATIONS FOR USE STATEMENT ### APPLICANT: Shun Thai Rubber Gloves Industry Public Company, Ltd. # 510(k) NUMBER (if known): K052030_ ### DEVICE NAME: Royal Guard Latex, Powder-Free, Surgeon's Glove - Sterile #### Indications For Use: The Royal Guard Latex, Powder-Free, Surgeon's Glove - Sterile, is a device made of The Royal Quard Latex, Forver 1100, Salgers by operating room personnel to natural '01 synthette rubber intended to so m. protect a surgical wound from contamination between patient and operating room personnel. Prescription Use ... ... ................ Per 21 CFR 801.109 AND/OR Over-The-Counter Use ... ... .............................. (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) | | Concurrentce of CDRH, Office of Device Evaluation (ODE) | | |----------------------------------------------|---------------------------------------------------------|--| | (Division Sign-Off) | | | | Division of Anesthesiology General Hospital, | | | | Infection Control, Dental Devices | | | | 510(k) Number | K052030 | | | | Revised 31 Aug 2005 | | | | | | atch " --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K052030](https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K052030) **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. 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