← Product Code [EKZ](/submissions/DE/subpart-e%E2%80%94surgical-devices/EKZ) · K052622 # MACAN MODEL MC-4A DENTAL ELECTROSURGICAL UNIT (K052622) _Macan Engineering Co. · EKZ · Dec 9, 2005 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EKZ/K052622 ## Device Facts - **Applicant:** Macan Engineering Co. - **Product Code:** [EKZ](/submissions/DE/subpart-e%E2%80%94surgical-devices/EKZ.md) - **Decision Date:** Dec 9, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.4920 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** Therapeutic ## Intended Use Soft tissue management within the oral cavity to address the indications for incision, excision and ess of the success in and caff to comboof ties o Soft tissue managements in intra-oral soft tissue. ## Device Story AC-powered dental electrosurgical unit; provides controlled power to cutting and coagulating electrodes. Operates by delivering electrical current from electrode tip into tissue; modes allow for soft tissue incision or coagulation. Used in oral cavity by dental professionals. Output affects clinical decision-making by enabling precise tissue management and bleeding control during surgery. Benefits patient through improved surgical access and hemostasis. ## Clinical Evidence No clinical data; substantial equivalence based on technological comparison to predicate device. ## Technological Characteristics AC-powered electrosurgical unit; includes controlled power source and interchangeable cutting/coagulating electrodes. Same materials and specifications as predicate device. ## Regulatory Identification A dental electrosurgical unit and accessories is an AC-powered device consisting of a controlled power source and a set of cutting and coagulating electrodes. This device is intended to cut or remove soft tissue or to control bleeding during surgical procedures in the oral cavity. An electrical current passes through the tip of the electrode into the tissue and, depending upon the operating mode selected, cuts through soft tissue or coagulates the tissue. ## Predicate Devices - MACAN -Regis MC6A (050735) ## 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}------------------------------------------------ K052622 #### DEC 9 2005 ## Original Premarket Approval Application for MACAN MC-4A 20 Sept 2005 ### 510(k) SUMMARY | 510(k) Owner :
Contact person : | Mickey Albergo ( Business Manager)
Rich Garrett ( Product Engineer ) | |------------------------------------|----------------------------------------------------------------------------------------------------------| | Business address: | MACAN Engineering and Manufacturing Co.
1564 N. Damen Ave.
Chicago, Ill. 60622
1-(773)-772-2000 | | Device Classification Name : | Unit, Electrosurgical, and Accessories, Dental | | Device Proprietary Trade Name : | MACAN model MC-4A Dental Electrosurgical Unit | | Regulation : | 872.4920 | | Product Code : | EKZ | | Classification : | class II | | Owner/Operator : | MACAN Engineering and Manufacturing Co. | | Owner/Operator Number : | 1418975 | Device description : The MC-4A dental electrosurgical unit is an AC powered device consisting of a controlled power source and a set of cutting and coagulating electrodes. The device is intended a controlled power of thissue or to control bleeding during surgery in the oral cavity. An electrical to our of the tip of the tip of the electrode into tissue and, depending upon the operating mode selected, either cuts through soft tissue or coagulates the tissue. Predicate Substantially Equivalent Device Legally Marketed : MACAN -Regis MC6A Unit, Electrosurgical, and Accessories, Dental Device Classification Name : 872.4920 Regulation : EKZ Product Code : class II Classification : 510(k) Number : 050735 #### SUMMARY TABLE OF COMPARISON | Indications for Use | SAME | |---------------------|----------------------------------------------| | Electrical Output | SAME RATINGS | | Electrodes | SAME
same manufacturer, same part numbers | | Accessories | SAME
same manufacturer, same part numbers | | Control Functions | SAME | It is reasonable to conclude, on the basis of the Summary Table of Comparison, that the MACAN model MC-4A dental electrosurgical unit is substantially equivalent to the cited predicate device. Note : the issue of electrode and hand piece material bio-compatibility is addressed within the submission for the predicate device. {1}------------------------------------------------ Image /page/1/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 text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol resembling an eagle or bird in flight, composed of three curved lines above two wavy lines. Public Health Service DEC 9 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Mickey Albergo Manager Macan Engineering Company 1564 North Damen Avenue Chicago, Illinois 60622 Rc: K052622 Trade/Device Name: MACAN Model MC-4A Dental Electrosurgery Unit Regulation Number: 872.4920 Regulation Name: Dental Electrosurgical Unit and Accessories Regulatory Class: II Product Code: EKZ Dated: September 20, 2005 Received: September 27, 2005 Dear Mr. Albergo: 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 eenurements 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 (1 wr 1), tends of be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, ITDA may publish further announcements concerning your device in the Federal Register. {2}------------------------------------------------ Page 2 - Mr. Albergo 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. or me rot of any ly 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 and ilouing (= = 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), nlease contact the Office of Compliance 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 maj overs 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 yours, Clus 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 {3}------------------------------------------------ # Indications for Use K052622 510(k) Number (if known): MACAN model MC-4A dental electrosurgery unit Device Name: Indications For Use: Soft tissue management within the oral cavity to address the indications for incision, excision and ess of the success in and caff to comboof ties o Soft tissue managements in intra-oral soft tissue. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Susan Runne Page 1 of *_*_ --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EKZ/K052622](https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EKZ/K052622) **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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