← Product Code [IWJ](/submissions/RA/subpart-f%E2%80%94therapeutic-devices/IWJ) · K972554 # REGANES RADIONUCLIDE SEED MAGAZINE (K972554) _Avid N.I.T., Inc. · IWJ · Feb 17, 1998 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/IWJ/K972554 ## Device Facts - **Applicant:** Avid N.I.T., Inc. - **Product Code:** [IWJ](/submissions/RA/subpart-f%E2%80%94therapeutic-devices/IWJ.md) - **Decision Date:** Feb 17, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.5650 - **Device Class:** Class 1 - **Review Panel:** Radiology - **Attributes:** Therapeutic ## Indications for Use A single patient use disposable device to hold radioactive seeds, in magazine fashion, in the MICK radionuclear 200-TP applicator. This device performs the same function as the reusable magazines sold by Mick Radionuclear Instruments, Inc. ## Device Story The Radionuclide Seed Magazine is a single-patient-use disposable device designed to hold radioactive seeds in a magazine configuration. It is intended for use with the MICK radionuclear 200-TP applicator. The device functions as a direct replacement for reusable magazines used in the same applicator system. It is operated by clinical staff during brachytherapy procedures to facilitate the delivery of radioactive seeds. By providing a disposable alternative to reusable magazines, the device aims to simplify clinical workflows and reduce the need for sterilization of seed-holding components. ## Clinical Evidence No clinical data; bench testing only. ## Technological Characteristics Disposable, single-patient-use magazine for radioactive seed delivery. Designed for mechanical compatibility with the MICK 200-TP applicator. No electronic, software, or energy-based components. ## Regulatory Identification A manual radionuclide applicator system is a manually operated device intended to apply a radionuclide source into the body or to the surface of the body for radiation therapy. This generic type of device may include patient and equipment supports, component parts, treatment planning computer programs, and accessories. ## Predicate Devices - Mick Radionuclear Instruments, Inc. reusable magazines ## 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}------------------------------------------------ Image /page/0/Picture/0 description: The image shows a circular logo with text around the perimeter and a symbol in the center. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES". The symbol in the center consists of three stylized lines that resemble a person with outstretched arms. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Joseph Harms President Needle & Infusion Technologies, Inc. 390 Scarlet Blvd. Oldsmar, Florida 34677 Re: FEB 17 1998 K972554 NIT Radionuclide Seed Magazine Dated: November 4, 1997 Received: November 19, 1997 Regulatory Class: I 21 CFR 892.5650/Procode: 90 IWJ Dear Mr. Harms: We have reviewed your Section 510(k) notification of intent to market the device and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, 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 prodibitions against misbranding and adulteration. If vour device is classified (see above) into either 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 requirement, as set forth in the Quality System Regulation (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 action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarker potification does not affect any obligation you might have under sections 531 through 542 of the Act for devices under 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 regulation (21 CFR Part 80) and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for question 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) 638-204) or -----(301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, h.7liau Yi Lillian Yin, Ph.D. Director, Division of Reproductive, Abdominal, Ear, Nose and Throat, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {1}------------------------------------------------ 1972554 510(k) Number (if known): Device Name: Radionuclide Seed Maqazine ## Indications For Use: ( A single patient use disposable device to hold radioactive seeds, in magazine fashion, in the MICK radionuclear 200-TP applicator. This device performs the same function as the reusable magazines sold by Mick Radionuclear Instruments, Inc. EXP : "BET" (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Harish A. Sagnier Division Sign Off (Division Sign-Off) (Division of Reproductive, Abdominal, El and Radiological Devic 510(k) Number **Prescription Use** (Per 21 CFR 801.109) ✓ OR Over-The-Counter Use (Optional Format 1-2-96) --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/IWJ/K972554](https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/IWJ/K972554) **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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