← Product Code [FPA](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA) · K082027 # FLU-ADMIN, MODELS 60150, 60150C, 60151C, 60153C, 60160 (K082027) _Genesis Bps, LLC · FPA · Feb 13, 2009 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K082027 ## Device Facts - **Applicant:** Genesis Bps, LLC - **Product Code:** [FPA](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA.md) - **Decision Date:** Feb 13, 2009 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 880.5440 - **Device Class:** Class 2 - **Review Panel:** General Hospital - **Attributes:** Therapeutic ## Indications for Use Intended to be used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. ## Device Story The FLU-ADMIN I.V. Set is a manual fluid delivery system consisting of a spike, drip chamber, tubing, roller clamp, "Y" injection site, and male luer slip. It functions by gravity-fed delivery of fluids from a container to a patient's vein. Most models deliver 20 drops/ml, while model 0151C delivers 60 drops/ml. Certain models include a check valve; most are vented, with the exception of model 0160. The device is used in clinical settings by healthcare professionals to facilitate intravenous therapy. It provides a controlled path for fluid administration, benefiting patients requiring hydration, medication, or nutritional support. ## Clinical Evidence Bench testing only. ## Technological Characteristics Manual gravity-fed intravascular administration set. Components include spike, drip chamber, PVC/plastic tubing, roller clamp, "Y" injection site, and male luer slip. Models vary by drop rate (20 or 60 drops/ml), presence of check valve, and venting status. Non-electronic, mechanical device. ## Regulatory Identification An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container. ## Special Controls *Classification.* Class II (special controls). The special control for pharmacy compounding systems within this classification is the FDA guidance document entitled “Class II Special Controls Guidance Document: Pharmacy Compounding Systems; Final Guidance for Industry and FDA Reviewers.” Pharmacy compounding systems classified within the intravascular administration set are exempt from the premarket notification procedures in subpart E of this part and subject to the limitations in § 880.9. ## Predicate Devices - FLU VEN I.V. SETS (K11914) - FLU VEN I.V. SET 0153-C ([K843692](/device/K843692.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}------------------------------------------------ tos2027 # Genesis BPS, LLC 510(k) Notification FLU-ADMIN I.V. SETS July 15, 2008 Page 4 ### 510(k) Summary FEB 1 3 2009 Applicant: Address Genesis BPS, LLC 65 Commerce Way Hackensack, NJ 07601 Contact Person: Address Telephone Fax Email Jerrold B. Grossman, Ph.D. President, Genesis BPS, LLC 65 Commerce Way Hackensack, NJ 07601 (201) 708-1400 (201) 708-1104 jgrossman@genesisbps.com Submission Correspondent: Telephone Fax Email Classification Name: Registration-Number !- Product code: Class: Carolyn Amditis, BSMT (ASCP) (201) 708-1400 (201) 708-1104 camditis@genesisbps.com Device Information: Trade Name: These devices will be marketed under the trade name FLU-ADMIN I.V. SETS Common/Usual Name: Intravascular Administration Set Set, Intravascular Administration (21 CFR 880.5440) | 99100000
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Intended to be used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. {1}------------------------------------------------ ## DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract image of an eagle. #### Public Health Service # FEB 1 3 2009 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Genesis BPS, LLC Ms. Carolyn Amditis, BSMT (ASCP) Manager, Technical Services & Quality Control 65 Commerce Way Hackensack, New Jersey 07601 K082027 Re: > Trade/Device Name: FLU-ADMIN I.V. Sets Regulation Number: 880.5440 Regulation Name: Intravascular Administration Set Regulatory Class: II Product Code: FPA Dated: January 28, 2009 Received: February 2, 2009 Dear Ms. Amditis: 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. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting vour 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. {2}------------------------------------------------ #### Page 2 - Ms. Amditis 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 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 begin 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 Center for Devices and Radiological Health's (CDRH's) 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/industry/support/index.html. Sincerely yours; -- Antony D. Auster for Ginette Y. Michaud, M.D Acting Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health {3}------------------------------------------------ # Genesis BPS, LLC 510(k) Notification FLU-ADMIN I.V. SETS AMENDMENT ## Indications for Use Statement ## 510(k): Device Name: FLU-ADMIN I.V. Sets Indications of Use: Genesis BPS FLU-ADMIN I.V. Sets are intended to be used to administer fluids from a container to a patient's vascular system through a needle or catheter into a vein. | Prescription Use | XX and/or Over-the-Counter Use | |-----------------------------|--------------------------------| | (Part 21 CFR 801 Subpart D) | (21 CFR 807 Subpart C) | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE AS NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) | (Division Sign-Off) | | |----------------------------------------------|---------| | Division of Anesthesiology, General Hospital | | | Infection Control, Dental Devices | | | 510(k) Number: | K082027 | --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K082027](https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K082027) **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