← Product Code [HIF](/submissions/OB/subpart-b%E2%80%94obstetrical-and-gynecological-diagnostic-devices/HIF) · K992381 # CO2 GAS WARMER II, MODEL 6-800-00 (K992381) _Northgate Technologies, Inc. · HIF · Sep 17, 1999 · Obstetrics/Gynecology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OB/subpart-b%E2%80%94obstetrical-and-gynecological-diagnostic-devices/HIF/K992381 ## Device Facts - **Applicant:** Northgate Technologies, Inc. - **Product Code:** [HIF](/submissions/OB/subpart-b%E2%80%94obstetrical-and-gynecological-diagnostic-devices/HIF.md) - **Decision Date:** Sep 17, 1999 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 884.1730 - **Device Class:** Class 2 - **Review Panel:** Obstetrics/Gynecology - **Attributes:** Therapeutic ## Indications for Use The Nortech CO2 Gas Warmer II Unit shall be used as a means of supplying warm gas for the distention of the abdomen for diagnostic and/or operative laparoscopy. ## Device Story CO2 Gas Warmer II is a laparoscopic accessory used to heat insufflation gas. System consists of a control unit, reusable heat exchanger, and power cords. Device connects to an insufflator to provide continuous, non-adjustable heating of CO2 gas to a target range of 35-40.5°C. Used in clinical settings (OR) by physicians during laparoscopic procedures to maintain patient body temperature and reduce potential thermal shock from cold gas. Output is warmed gas delivered to the abdominal cavity. Benefits include improved patient comfort and potential reduction in hypothermia risks during surgery. ## Clinical Evidence No clinical data provided; substantial equivalence is based on design and material characteristics. ## Technological Characteristics System comprises a control unit and reusable heat exchanger. Materials are non-toxic and previously used in medical devices. Provides continuous, non-adjustable heating of gas to 35-40.5°C. Powered by electrical cords. ## Regulatory Identification A laparoscopic insufflator is a device used to facilitate the use of the laparoscope by filling the peritoneal cavity with gas to distend it. ## Reference Devices - Snoden Pencer (similar device) - Wisap (similar device) ## 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}------------------------------------------------ SEP 1 7 1999 # SUMMARY OF SAFETY AND EFFECTIVENESS Insufflator, Laparoscopic Accessory Common/Usual Name: CO., Gas Warmer II Proprietary Name: Classification: Class II #### Materials: All materials used to manufacture the Northgate Technologies Inc. CO3 Gas Warmer II Unit are non-toxic and have been previously used to manufacture other medical devices. ## Description: The CO, Gas Warmer II Unit is designed to be used in conjunction with an insufflator to provide continuous non-adjustable heating of gas to a laparoscopic instrument. The CO2 Gas Warmer II Unit is comprised of a control unit and reusable heat exchanger and power cords. ## Substantial Equivalence: Northgate's CO2 Gas Warmer II Unit which is comprised of a control unit/heat exchanger and power cords are substantially equivalent in design, materials, and intended use to numerous currently marketed devices. Other manufacturers of similar devices are Snoden Pencer and Wisap. ## Intended Use: The Nortech CO2 Gas Warmer II Unit shall be used as a means of supplying warm gas for the distention of the abdomen for diagnostic and/or operative laparoscopy. {1}------------------------------------------------ Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 SEP 1 7 1999 Mr. Casey Kurek Requlatory Manager Northgate Technologies Incorporated 600 Church Road Elgin, IL 60123 . Re: K992381 CO2 Gas Warmer II Dated: August 16, 1999 Received: August 19, 1999 Requiatory Class: Il 21 CFR §884.1730/Procode: 85 HIF Dear Mr. Kurek: 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 regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General requlation (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 action. In addition. 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 sections 531 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), piease 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"(21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers 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, CAPT Daniel G. Schultz, M.D. Acting Director, Division of Reproductive, Abdominal, Ear, Nose and Throat, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ Page 1 of 1 Confidential 510(k) Number (if known K992381 Device Name: CO2 Gas Warmer II Indications For Use: THE NORTECH GAS WARMER II IS INDICATED FOR WARMING GAS (95-1059F/35-40.5°C) USED FOR THE DISTENTION OF THE ABDOMEN FOR DIAGNOSTIC AND/OR OPERATIVE LAPAROSCOPY. Cury Kurek C. Kurek, Regulatory Manager C. Kurek, Regulatory Manager (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use X (Per 21 CFR 801.109) OR Over-the-Counter Use (Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices 510(k) Number K992381 (Optional Format 1-2-96) --- **Source:** [https://fda.innolitics.com/submissions/OB/subpart-b%E2%80%94obstetrical-and-gynecological-diagnostic-devices/HIF/K992381](https://fda.innolitics.com/submissions/OB/subpart-b%E2%80%94obstetrical-and-gynecological-diagnostic-devices/HIF/K992381) **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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