← Product Code [OMP](/submissions/SU/subpart-e%E2%80%94surgical-devices/OMP) · K052456 # MODIFICATION TO VERSATILE 1 WOUND VACUUM SYSTEM (K052456) _Blue Sky Medical Group Incorporated · OMP · Nov 4, 2005 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OMP/K052456 ## Device Facts - **Applicant:** Blue Sky Medical Group Incorporated - **Product Code:** [OMP](/submissions/SU/subpart-e%E2%80%94surgical-devices/OMP.md) - **Decision Date:** Nov 4, 2005 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 878.4780 - **Device Class:** Class 2 - **Review Panel:** General, Plastic Surgery - **Attributes:** Therapeutic ## Intended Use The Versatile 1TM Wound Vacuum System is indicated for patients who would benefit from a suction device particularly as the device may promote wound healing or for aspiration and removal of surgical fluids, tissue (including bone), gases, bodily fluids or infectious materials from a patients airway or respiratory support system either during surgery or at the patients bedside. ## Device Story Portable suction pump; used for general drainage or wound healing promotion via accessory wound sealing kits. Operates by applying negative pressure to wound sites or airway/respiratory systems. Used in surgical settings or at patient bedside; operated by clinicians. Output consists of suction force; assists in fluid/tissue removal and wound management. Benefits include potential promotion of wound healing and effective aspiration of materials from respiratory systems. ## Clinical Evidence No clinical data; bench testing only. ## Technological Characteristics Portable suction pump; powered device. Materials modified from predicate; sterilization parameters unchanged. Operates via vacuum suction. Standalone device. ## Regulatory Identification A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter. ## Predicate Devices - Versatile 1TM Wound Vacuum System ([K042134](/device/K042134.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}------------------------------------------------ K052456 NOV - 4 2005 ## 510(k) Summary # General Information Submitters Name/Address: BlueSky Medical Group, Inc. 5924 Balfour Ct., Suite D Carlsbad, CA 92008 | Establishment Registration Number: | 2032666 | |------------------------------------|-----------------| | Contact Person: | Jasper Benke | | Phone Number: | (760) 603-8130 | | Date Prepared: | August 30, 2005 | Device Description | Trade Name: | Versatile 1™ Wound Vacuum System | |----------------------|----------------------------------------------------------| | Generic/Common Name: | Suction Pump and Accessories | | Classification Name: | Powered Suction Pump (21 CFR 878.4780, Product Code BTA) | ## Predicate Device Information Versatile 1TM Wound Vacuum System. K042134; cleared on November 15, 2004 ## Product Description The product is a portable suction pump for general purpose drainage or for the promotion of wound healing when used with various accessory wound sealing kits. #### Intended Use The Versatile 1TM Wound Vacuum System is indicated for patients who would benefit from a suction device particularly as the device may promote wound healing or for aspiration and removal of surgical fluids, tissue (including bone), gases, bodily fluids or infectious materials from a patients airway or respiratory support system either during surgery or at the patients bedside. ### Substantial Equivalence This Special 510(k) proposes a modification in materials and labeling for the Versatile 1 TM Wound Vacuum System, which were previously cleared under K042134 on November 15, 2004. The indications for use, technology, principle of operation, packaging, and sterilization parameters of the device remain the same as in the predicate cleared 510(k). #### Summary of Safety and Effectiveness The modified Versatile 1TM Wound Vacuum System, as described in this submission, is substantially equivalent to the predicate, unmodified device. The proposed modifications in materials and labeling are not substantial changes or modifications, and do not significantly affect the safety or efficacy of the 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 stylized eagle-like symbol, with its wings forming a curved shape. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES. USA" is arranged in a circular fashion around the symbol. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 APR - 7 2009 Smith & Nephew, Inc. % Ms. Laura Krejci 970 Lake Carillon Drive, Suite 110 St. Petersburg, Florida 33716 Re: K052456 Trade/Device Name: Versatile 1™ Wound Vacuum System Regulation Number: 21 CFR 878.4780 Regulation Name: Powered Suction Pump Regulatory Class: II Product Code: OMP Dated: October 19, 2005 Received: October 21, 2005 Dear Ms. Krejci: This letter corrects our substantially equivalent letter of November 4, 2005. 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 (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. 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 {2}------------------------------------------------ Page 2 - Ms. Laura Krejci limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); 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. This letter will allow you to continue 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), please 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). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Postmarket Surveillance at (240) 276-3474. For questions regarding the reporting of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at (240) 276-3464. 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html. Sincerely yours, Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## Indications for Use K052456 510(k) Number: Versatile 1 ™ Wound Vacuum System Device Name: Indications for use: The Versatile 1 Wound Vacuum System is indicated for patients who would benefit from a suction device particularly as the device may promote wound healing or for aspiration and removal of surgical fluids, tissue (including bone), gases, bodily fluids or infectious materials from a patients airway or respiratory support system either during surgery or at the patients bedside. Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Marlene Buell Restorative. and Neurological Devices Page 1 of ____________________________________________________________________________________________________________________________________________________________________ 510(k) Number K052456 --- **Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OMP/K052456](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OMP/K052456) **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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