← Product Code [EGS](/submissions/DE/subpart-e%E2%80%94surgical-devices/EGS) · K022264 # CLEAN 'N' OIL (K022264) _Svenska Dental Instruments AB · EGS · Oct 2, 2002 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGS/K022264 ## Device Facts - **Applicant:** Svenska Dental Instruments AB - **Product Code:** [EGS](/submissions/DE/subpart-e%E2%80%94surgical-devices/EGS.md) - **Decision Date:** Oct 2, 2002 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.4200 - **Device Class:** Class 1 - **Review Panel:** Dental ## Intended Use Clean'n'Oil is a maintenance spray for lubrication and cleaning of Turbines, Straight and Contra-Angled Handpieces, Air-Scalers and Air-Motors. ## Device Story Clean'n'Oil is a maintenance spray designed for dental clinical environments. It is used by dental professionals to lubricate and clean dental handpieces, including turbines, straight and contra-angled handpieces, air-scalers, and air-motors. The device functions as a mechanical maintenance tool to ensure proper operation and longevity of dental instruments. It does not involve electronic processing, software, or automated analysis. ## Clinical Evidence Bench testing only. ## Technological Characteristics Maintenance spray for dental handpieces. Mechanical lubrication and cleaning agent. No electronic components, software, or energy source. ## Regulatory Identification A dental handpiece and accessories is an AC-powered, water-powered, air-powered, or belt-driven, hand-held device that may include a foot controller for regulation of speed and direction of rotation or a contra-angle attachment for difficult to reach areas intended to prepare dental cavities for restorations, such as fillings, and for cleaning teeth. ## 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}------------------------------------------------ ### DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/0/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal is circular, with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. In the center of the seal is a stylized image of an eagle with three lines extending from its head. #### Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 # OCT 0 2 2002 Ms. Emma Bergquist Product and Quality Co-Ordinator Svenska Dental Instruments AB Finvids väg 8 P.O. Box 723 SE-194 27 Upplands Väsby SWEDEN Re: K022264 Trade/Device Name: Clean 'n' Oil Regulation Number: 872.4200 Regulation Name: Dental Handpiece and Accessories Regulatory Class: I Product Code: EGS Dated: July 1, 2002 Received: July 12, 2002 Dear Ms. Bergquist: 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 vour 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. {1}------------------------------------------------ Page 2 – Ms. Bergquist 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. 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 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613 . Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division 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.qov/cdrh/dsma/dsmamain.html Sincerely yours Timothy A. Ulatowski Director Division of Anesthesiology, General Hospital. Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health {2}------------------------------------------------ 5 10(k) | Jumbe : ## K022264 Clean'n'Oil [Jevice Name: Indicati ans Fo · Use: Clean'n'Oil is a maintenance spray for lubrication and cleaning of Turbines, Straight and Contra-Angled Handpieces, Air-Scalers and Air-Motors. (PLE ASE DO NOT WRITE BELOW THIS LINE -- CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Division of Anesthesiology, General Hospital, Infection Control, Dental Devices 510(k) Number: K033064 > Pre :criptio \ Use: _ (Pe 21CFIR 801.109) Over -the-Counter Use: __ (Optional format 1-2-96) ### Svonska Dental Instrument AB P.C. Box 723 SE 194 27 Upplands Väsby SW EDEN Phone No +46-8-506 505 75 +46-8-506 505 83 Direct line E-mail order and information E-mail Web site OR +46-8-590 306 30 Telefax No VAT-No SE556013882701 info@sdidirecta.com emma.bergquist@sdidirecta.com www.sdidirecta.com --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGS/K022264](https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGS/K022264) **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