← Product Code [GCJ](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/GCJ) · K122526 # 360 GAS ASSISTED ENDOSCOPIC APPLICATOR (K122526) _Micromedics, Inc. · GCJ · Nov 16, 2012 · Gastroenterology, Urology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-b%E2%80%94diagnostic-devices/GCJ/K122526 ## Device Facts - **Applicant:** Micromedics, Inc. - **Product Code:** [GCJ](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/GCJ.md) - **Decision Date:** Nov 16, 2012 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 876.1500 - **Device Class:** Class 2 - **Review Panel:** Gastroenterology, Urology ## Indications for Use The 360° Gas Assisted Endoscopic Applicator is intended for the application of two non-homogenous fluids. ## Device Story Sterile, single-use, disposable endoscopic applicator; used for delivery of two non-homogeneous liquids. Device features two proximal luer connectors for syringe attachment and one connector for compressed air/inert gas power source. Distal end incorporates flexible Pebax tube for directional tip positioning. Operated by clinicians in endoscopic procedures. Gas assistance facilitates fluid application. Benefits include controlled, directional delivery of fluids during endoscopic interventions. ## Clinical Evidence Bench testing only. Evaluation included biocompatibility (ISO 10993-1), pull/torque testing, leak testing, spray testing, mixing tests, sterilization validation, and shelf-life evaluation. All test articles met pre-defined acceptance criteria. ## Technological Characteristics Materials include Pebax (distal tube). Device is a sterile, single-use, disposable endoscopic applicator. Features two luer connectors for fluid input and one connector for gas power source. Sterilized via ethylene oxide. Packaged in PETG tray/Tyvek lid. No software or electronic components. ## Regulatory Identification An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations. ## Special Controls *Classification* —(1)*Class II (special controls).* The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9. ## Predicate Devices - Air Assisted Endoscopic Applicator ([K042834](/device/K042834.md)) ## 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}------------------------------------------------ Special 510(k) Premarket Notification 360° Gas Assisted Endoscopic Applicator Image /page/0/Picture/2 description: The image shows the text "K122526" in a handwritten style. The text is written in black ink on a white background. The numbers are slightly stylized, with the "2" having a curved shape. 510(K) Summary NOV 1 6 2012 Date Prepared: October 12, 2012 | 510(k) Submitter | Contact for Official Correspondence | |---------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------| | Micromedics, Inc.
1270 Eagan Industrial Road, Suite 120
St. Paul, MN 55121-1385 | Jodi L. Raus, MBA, RAC
Tel: 651-452-1977; Fax: 651-452-1787
Email: jodi.raus@nordsonmicromedics.com | | General Information | | | | |-------------------------------|--------------------------------------------------------------------------|--------------|---------------------------| | Trade Name | 360° Gas Assisted Endoscopic
Applicator | Common Name | Endoscopic Applicator | | Classification
Information | Endoscope and accessories
per 21 CFR 876.1500 (Class II) | Product Code | GCJ | | | | Panel | General & Plastic Surgery | | Predicate
Devices | Air Assisted Endoscopic Applicator, K042834 cleared on February 11, 2005 | | | #### Device Description The 360° Gas Assisted Endoscopic Applicator is a sterile, single-use, disposable device intended for the application of two non-homogeneous liquids. The 360° Gas Assisted Endoscopic Applicator is designed with two luer connectors at the proximal end, which is used for connection to two syringes containing the non-homogeneous liquids. There is also a connector at the proximal end to be attached to a tubing set which is connected to a compressed air/inert gas power source. The 360° Gas Assisted Endoscopic Applicator is packaged with an air line with filter in a PETG tray/Tyvek lid configuration and sterilized using ethylene oxide. Five individually sterile packaged applicators are contained in a shelf carton along with the instructions for use. ## Intended Use / Indications The 360° Gas Assisted Endoscopic Applicator is intended for the application of two non-homogenous fluids. ## Substantial Equivalence Comparison The endoscopic applicator subject to this special 510(k) incorporates a flexible Pebax tube at the distal end of the applicator which allows for directional positioning of the tip. #### Summary of Non-Clinical Performance Data The 360° Gas Assisted Endoscopic Applicator was evaluated through design verification and biocompatibility testing. Biocompatibility testing performed in accordance with ISO 10993 - Biological evaluation of medical devices, Part 1 – Evaluation and tests (2009) show the device is considered safe for use for its intended biocontact. Non-clinical testing included the tests listed below and showed the test articles met the pre-defined acceptance criteria, therefore demonstrating the mechanical integrity and suitability of the device for its intended use over the labeled shelf life. - Pull (Torque) Testing . - Leak Testing . - . Spray Testing - Mixing Test . - . Sterilization Validation - Shelf life Evaluation . {1}------------------------------------------------ Special 510(k) Premarket Notification 360° Gas Assisted Endoscopic Applicator ## Substantial Equivalence Conclusion Substantial Equivalence Collection The 360° Gas Assisted Endoscopic Applicator does not raise new questions of safety or effectiveness when compared to the predicate devices and is, therefore, substantially equivalent. - The remainder of this page intentionally left blank.- {2}------------------------------------------------ ## DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002 November 16, 2012 Micromedics, Incorporated % Ms. Jodi Raus MBA, RAC Director of Regulatory, Clinical and Quality Affairs 1270 Eagan Industrial Road, Suite 120 Saint Paul, Minnesota 55121 Re: K122526 Trade/Device Name: 360° Gas Assisted Endoscopic Applicator Regulation Number: 21 CFR 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: II Product Code: GCJ Dated: October 17, 2012 Received: October 18, 2012 Dear Ms. Raus: 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 {3}------------------------------------------------ Page 2 - Ms. Jodi Raus MBA, RAC CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucml15809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely yours, # David Krause Mark N. Melkerson Acting Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ Micromedics, Inc Special 510(k) Premarket Notification 360° Gas Assisted Endoscopic Applicator ## Attachment 2 # Indications for Use Statement Continued of the commend of the comments of the comments of the production of the comments of ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ 510(k) Number: K122526 360° Gas Assisted Endoscopic Applicator Device Name The 360° Gas Assisted Endoscopic Applicator is intended for the Indications application of two non-homogenous fluids. for Use OR Prescription Use _ X (Per 21 CFR 801. 109) Over-The-Counter Use # PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED Concurrence of CDRH, Office of Device Evaluation (ODE) Rinut for MXM (Division Sign-Off) Division of Surgical Devices K122526 510(k) Number_ --- **Source:** [https://fda.innolitics.com/submissions/SU/subpart-b%E2%80%94diagnostic-devices/GCJ/K122526](https://fda.innolitics.com/submissions/SU/subpart-b%E2%80%94diagnostic-devices/GCJ/K122526) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com