← Product Code [KGO](/submissions/SU/subpart-e%E2%80%94surgical-devices/KGO) · K050533 # ECLIPSE LATEX POWDER FREE STERILE SURGEON'S GLOVE (K050533) _Regent Medical Americas, LLC · KGO · Apr 26, 2005 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K050533 ## Device Facts - **Applicant:** Regent Medical Americas, LLC - **Product Code:** [KGO](/submissions/SU/subpart-e%E2%80%94surgical-devices/KGO.md) - **Decision Date:** Apr 26, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 878.4460 - **Device Class:** Class 1 - **Review Panel:** General, Plastic Surgery ## Intended Use A powder-free sterile surgeon's glove is a disposable device made of latex that is intended to be worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants. ## Device Story Eclipse Latex Powder Free Sterile Surgeon's Glove is a disposable, sterile, latex-based protective barrier. Designed for use in surgical settings by healthcare professionals to prevent cross-contamination between the wearer and the patient. The device functions as a physical barrier against infectious materials and contaminants. It is a single-use, non-implantable medical device. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Material: Latex. Form factor: Sterile, powder-free surgeon's glove. Classification: Class I, Product Code KGO, Regulation 878.4460. ## 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 the HHS seal, which features an abstract image of an eagle with three lines representing its wings. The seal is surrounded by the text "DEPARTMENT OF HEALTH AND HUMAN SERVICES USA" in a circular arrangement. Public Health Service APR 2 6 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Ms. Kathleen Harris Global Regulatory Manager Regent Medical Americas, LLC 3585 Engineering Drive, Suite 250 Norcross, Georgia 30092 Re: K050533 Trade/Device Name: Eclipse Latex Powder Free Sterile Surgeon's Glove Regulation Number: 878.4460 Regulation Name: Surgeon's Glove Regulatory Class: I Product Code: KGO Dated: March 31, 2005 Received: April 7, 2005 Dear Ms. Harris: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your becally a see ice is substantially equivalent (for the referenced above and nave determinou re) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Interstate connineree proct to that have been reclassified in accordance with the provisions of Amendinents, or to de rises that in to Act (Act) that do not require approval of a premarket the rederal I ood, Drug, and Comers , therefore, market the device, subject to the general approvin appreation (the Act. The general controls provisions of the Act include controls provisions of the Fea. " Insting 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 If your device is classified (see as 107.0) in the such and or regulations affecting (PMA), it may of subject to sach adam Regulations, Title 21, Parts 800 to 898. In your device can be found in the Court in the Courcements concerning your device in the Federal Register. {1}------------------------------------------------ ## Page 2 - Ms. Harris Please be advised that FDA's issuance of a substantial equivalence determination does not Please be advisod that 1 DTC issumes on that your device complies with other requirements mean that I DA has made a aves and regulations administered by other Federal agencies. of the Act of ally I oderal but sequirements, including, but not limited to: registration r out must comply with an the Fiel s rig (21 CFR Part 801); good manufacturing practice and listing (21 CFR Part 067), laceling systems (QS) regulation (21 CFR Part 820); and if requirents as set form in the quality spotsions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) This letter will anon your be began finding of substantial equivalence of your device to a premiarket notification. - The Fire 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), If you desire specific advice to: Jour at (240) 276-0115. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the may obtain of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely vours, Smitte Michian Crnit 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 510(k) Number (if known): Device Name: Eclipse latex powder free sterile surgeon's glove Indications For Use: A powder-free sterile surgeon's glove is a disposable device made of latex that is A power of co sterile but chands, usually in surgical settings, to provide a barrier the new a or ou never ous materials and other contaminants. Prescription Use · (Part 21 CFR 801 Subpart D) Over-The-Counter Use_ × (21 CFR 801 Subpart C) Page 1 of 1 (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) AND/OR Concurrence of CDRH, Office of Device Evaluation (ODE) Shila H. Migday 42 insion Sign-Off) Civision of Anesthesiology General Hospital, Infection Control, Dental Devices c10(k) Number: K050533 --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K050533](https://fda.innolitics.com/submissions/HO/subpart-e%E2%80%94surgical-devices/KGO/K050533) **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