← Product Code [EFB](/submissions/DE/subpart-e%E2%80%94surgical-devices/EFB) · K012308 # KAVO QUATTROCARE (K012308) _Kavo America · EFB · Jun 26, 2002 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EFB/K012308 ## Device Facts - **Applicant:** Kavo America - **Product Code:** [EFB](/submissions/DE/subpart-e%E2%80%94surgical-devices/EFB.md) - **Decision Date:** Jun 26, 2002 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.4200 - **Device Class:** Class 1 - **Review Panel:** Dental ## Intended Use KaVo QUATTROcare is intended for internal cleaning, i.e., purging of old lubricant, for the maintenance of rotating dental and surgical instruments. NOTE: QUATTROcare should be used with only pre-cleaned dental handpieces and before they are sterilized. CAUTION: Federal (US) law restricts the use of this device to licensed professionals. ## Device Story KaVo QUATTROcare is an aerosol-based maintenance system for dental and surgical handpieces; utilizes pressurized cans containing hydrocarbon propellants, lubricants, and flavor/odor agents. Device performs internal cleaning by purging old lubricant from handpieces. Used in dental clinical settings by licensed professionals; applied to pre-cleaned instruments as a mandatory step prior to sterilization. System ensures proper instrument lubrication and debris removal, extending instrument life and maintaining hygiene standards. ## Clinical Evidence No clinical data. Substantial equivalence is based on performance data comparing formulations and intended uses to the predicate device. ## Technological Characteristics Aerosol-based maintenance system; consists of unit (2104 A) and pressurized cans (2106 A). Contains hydrocarbon propellants, lubricants, and flavor/odor ingredients. Manual application process for dental handpiece maintenance. ## 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. ## Predicate Devices - KaVo Spray ## 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}------------------------------------------------ # JUN 2 6 2002 K012308 ## SECTION 9 ### 510(k) SUMMARY This 510(k) summary of safety and effectiveness for KaVo QUATTROcare (unit and pressurized cans) is submitted in accordance with the requirements of SMDA 1990 and follows Office of Device Evaluation guidance concerning the organization and content of a 510(k) summary. - KaVo America Applicant: - 340 East Main Street Address: Lake Zurich, IL 60045 - Manufacturer: KaVo Dental GmbH Bahnhofstr. 20 D-8847 Warthausen Biberach GERMANY - Contact Person: Mr. John Westermeier - Telephone: 847-550-6800 847-550-6825 (Fax) 800-323-8029 - February 2002 Preparation Date: (of the Summary) KaVo QUATTROcare (Unit 2104 A; 6-pack of pressurized cans 2106 A) Device Name: - Dental Handpiece Accessory (for maintenance; cleaning, and lubrication) Common Name: Classification: Accessory to Dental Handpieces (Class I medical device: (21 CFR 872,4200), > Product Code: EFB (Product Code for Dental Handpieces) Panel: 76 Predicate devices: KaVo Spray Description: The KaVo QUATTROcare is an aerosol product with hydrocarbon propellants and lubricant and flavor/odor ingredients for use in the routine maintenance (cleaning and lubrication) of dental handpieces prior to their sterilization. {1}------------------------------------------------ - Indications: KaVo QUATTROcare is intended for internal cleaning, i.e., purging of old lubricant, for the maintenance of rotating dental and surgical instruments . NOTE: QUATTROcare should be used only with pre-cleaned dental handpieces and before they are sterilized. CAUTION: Federal (US) law restricts the use of this device to licensed professionals. - None required. The claim of substantial equivalence is based on Performance Data: comparisons of formulations and intended uses of the QUATTROcare and its claimed predicate. - CONCLUSION: Based on the information in the notification KaVo America believes that QUATTROcare is substantially equivalent to the claimed predicate (i.e., KaVo Spray, a pre-amendments product). Rev. April 2002 {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized symbol that resembles three human profiles facing to the right, with flowing lines suggesting movement or progress. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 # JUN 2 6 2002 Mr. John Westermeir Kavo America 340 East Main Street Lake Zurich, Illinois 60045 Re: K012308 Trade/Device Name: KaVo QUATTROcare Regulation Number: 872.4200 Regulation Name: Dental Handpiece and Accessories Regulatory Class: I Product Code: EFB Dated: April 12, 2002 Received: April 17, 2002 Dear Mr. Westermeier: 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 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. {3}------------------------------------------------ Page 2 - Mr. Westermeier 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.gov/cdrh/dsma/dsmamain.html Sincerely yours, Klatruds Timothy A. Ulatowski Timothy A. Ulatowski Director Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ### SECTION 7 ### INDICATIONS FOR USE STATEMENT 510(k) Number (if known): K012308 - Device Name: KaVo QUATTROcare Indications for Use Statement: KaVo QUATTROcare is intended for internal cleaning, i.e., purging of old lubricant, for the maintenance of rotating dental and surgical instruments. NOTE: QUATTROcare should be used with only pre-cleaned dental handpieces and before they are sterilized. KaVo proposes that KaVo QUATTROcare carry the following label: CAUTION: Federal (US) law restricts the use of this device to licensed professionals. Rev. April 2002 (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation Prescription Use کر (Per 21 CFR 801.109) OR Over-The Counter Use Susan Pum (Division Sign-Off) Division of Dental, Infection Control, and General Hospital, Infection Control, and General Hospi 510(k) Number --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EFB/K012308](https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EFB/K012308) **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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