ERBOTOM ICC 200

K933157 · Erbe USA, Inc. · GEI · Feb 23, 1994 · General, Plastic Surgery

Device Facts

Record IDK933157
Device NameERBOTOM ICC 200
ApplicantErbe USA, Inc.
Product CodeGEI · General, Plastic Surgery
Decision DateFeb 23, 1994
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 878.4400
Device ClassClass 2
AttributesTherapeutic

Device Story

The Erbotom ICC 200 is a high-frequency (HF) surgical generator designed for cutting and coagulating biological tissue. It utilizes the thermal effects of electric current to perform surgical procedures. The device is intended for use by clinicians in surgical settings. It incorporates safety features to protect patients and users from inadvertent injury. The device is an evolution of previous ERBE HF surgical instruments, designed to provide continuous improvement in surgical application, quality, and safety.

Clinical Evidence

No clinical data provided; bench testing and safety certifications (TUV and UL) are referenced as the basis for safety and effectiveness.

Technological Characteristics

High-frequency surgical generator; utilizes electric current for thermal tissue cutting and coagulation. Includes integrated safety devices for patient/user protection. Subject to TUV and UL safety approvals.

Indications for Use

Indicated for cutting and/or coagulation of biological tissue using high-frequency electric current.

Regulatory Classification

Identification

An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.

Predicate Devices

Submission Summary (Full Text)

{0} 4042021015 P.06 Amendment to: 510(k) Notification K933157 Erbotom ICC 200 July 21, 1993 2/23/94 MICHAEL A CLARK 775 Oxford Hall Dr. Lawrenceville, Georgia 30244 (404) 995 5720 SOUTH EAST REGULATORY ASSOCIATES Summary of Safety and Effectiveness This 510(k) summary of safety and effectiveness information is being submitted in accordance with the requirements of SIDA 1990. For more than 50 years, high-frequency (HF) surgery has been used to cut and/or coagulate biological tissue using the intrinsic thermal effect of electric current. ERBE has been working intensively during this entire period in the production of state-of-the-art HF surgical instruments. The ICC 200 represents one of the latest of these instruments. It is based upon ERBE's aim of continuous improvement in the application of HF surgical instruments and the quality and safety of cutting and coagulation of biological tissue. ERBE has successfully marketed the FDA approved FCC 450 unit. The ICC 200 is designed and constructed utilizing the same technical features as the ACC 450. In common with all ERBE equipment, the ICC 200 will carry TUV and UL approvals prior to introduction into the marketplace. ERBE's HF surgical instruments are all equipped with safety devices to protect both the patient and user against inadvertent injury. Michael A. Clark Michael A. Clark {1} DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service FEB 23 1994 Food and Drug Administration 1390 Piccard Drive Rockville MD 20850 Erbe USA, Inc. c/o Mr. Michael A. Clark South East Regulatory Associates 775 Oxford Hall Drive Lawrenceville, Georgia 30244 Re: K933157 Erbotom ICC 200 Regulatory Class: II Dated: November 19, 1993 Received: November 22, 1993 Dear Mr. Clark: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments. You may, therefore, market the device, subject to the general controls provisions of the Federal Food, Drug, and Cosmetic Act (Act). The general controls provisions of the Act include requirements for registration, listing of devices, good manufacturing practice, and labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval) 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 895. In addition, the Food and Drug Administration (FDA) may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under the Radiation Control for Health and Safety Act of 1968, or other Federal Laws or Regulations. This letter immediately will allow you to begin marketing your device as described. An FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and permits your device to proceed to the market, but it does not mean that FDA approves your device. Therefore, you may not promote or in any way represent your device or its labeling as being approved by FDA. If you desire specific advice on the {2} Page 2 - Mr. Michael A. Clark labeling for your device, please contact the Office of Compliance, Promotion and Advertising Policy Staff (HFZ-326) at (301) 594-4639. Other general information on your responsibilities under the Act, may be obtained from the Division of Small Manufacturers Assistance at their toll free number (800) 638-2041 or at (301) 443-6597. Sincerely yours, Paul R. Beninger, M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health 2
Innolitics
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