BIO-2000

K973765 · Micrylium Laboratories · EIA · Nov 4, 1998 · Dental

Device Facts

• Record ID: K973765
• Device Name: BIO-2000
• Applicant: Micrylium Laboratories
• Product Code: EIA · Dental
• Decision Date: Nov 4, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 872.6640
• Device Class: Class 1

Intended Use

For use in pressurized self-contained water devices. For use in cleaning lines in dental units by leaving the solution (Bio2000), dispensed by a pressurized device, overnight (similar period of time) or use continuously. Cleaning lines refers to the reduction of microbial contamination. For use in operative procedures to dedicated coolant (water) line for air or electric driven handpieces and scalers. Use of this device and solution will increase cutting efficiency and decrease the bad odors and tastes that occur during operative procedures while decreasing microbial contamination of the lubing.

Device Story

Bio-2000 is a solution dispensed via pressurized self-contained water devices in dental settings. It is used to clean dental unit waterlines by continuous or overnight application. The solution acts as a cleaner for coolant lines supplying air/electric handpieces and scalers. By reducing microbial contamination within the tubing, the device improves cutting efficiency and mitigates unpleasant odors and tastes during dental procedures. It is intended for use by dental professionals in clinical environments.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Chemical solution for dental unit waterline maintenance; dispensed via pressurized self-contained water systems.

Indications for Use

Indicated for use in dental unit waterlines to reduce microbial contamination, improve cutting efficiency, and eliminate odors/tastes during operative procedures involving air or electric driven handpieces and scalers.

Regulatory Classification

Identification

A dental operative unit and accessories is an AC-powered device that is intended to supply power to and serve as a base for other dental devices, such as a dental handpiece, a dental operating light, an air or water syringe unit, and oral cavity evacuator, a suction operative unit, and other dental devices and accessories. The device may be attached to a dental chair.

Submission Summary (Full Text)

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

4 1998 NOV

Dr. Thad Overmyer Micrylium Laboratories Suite 118 1755 West University Drive Phoenix Tempe), Arizona 85281

Re : K973765 Bio-2000 Trade Name: Regulatory Class: I Product Code: EIA Dated: September 16, 1998 Received: October 2, 1998

Dear Dr. Overmyer:

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 (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). 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 (Premarket Approval), it may be subject to such additional controls. Existing major requlations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. ਦੇ substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Requlation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory In addition, FDA may publish further announcements action. 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 sections 531

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Page 2 - Dr. Overmyer

through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

This letter will allow you to begin marketing your device as described in your 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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the requlation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other qeneral information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address

"http://www.fda.gov/cdrh/dsma/dsmamain.html".

Sincerely yours,

Timothy A. Ulatowski

Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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## Micrylium Laboratories

1755 West University Drive Suite 118 Phoenix (Tempe) Arizona 85281

TEL [phone]-1481 FAX (602) [e-mail] eMAIL

510 K ........................................................................................................................................................................

8102000

## INDICATIONS FOR USE

For use in pressurized self-contained water devices. 1.

For use in cleaning lines in dental units by leaving the solution 2. (Bio2000), dispensed by a pressurized device, overnight (similar period of time) or use continuously. Cleaning lines refers to the reduction of microbial contamination.

For use in operative procedures to dedicated coolant (water) line for air 3. or electric driven handpieces and scalers. Use of this device and solution will increase cutting efficiency and decrease the bad odors and tastes that occur during operative procedures while decreasing microbial contamination of the lubing.

Micrylium Laboratories

Do not write below this line

4————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————————— Concurrence of CDRH, Office of Device Evaluation (ODE)

Susan Quarr

(Division Sign-Off) Division of Dental, Infection Control, and General Hospital, Infection of

510(k) Number

Prescription Use (Per 12 CFR 801.109)

V

OR

Over the Counter Use (Optional Format 1-2-96)

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