← Product Code [JAF](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAF) · K973336 # IMEX STETHODOP (K973336) _Imex Medical Systems, Inc. · JAF · Feb 5, 1998 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAF/K973336 ## Device Facts - **Applicant:** Imex Medical Systems, Inc. - **Product Code:** [JAF](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAF.md) - **Decision Date:** Feb 5, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.1540 - **Device Class:** Class 2 - **Review Panel:** Radiology ## Intended Use Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: ## Device Story IMEX StethoDop is a Doppler ultrasound device used for diagnostic imaging or fluid flow analysis. It utilizes a 5 MHz transducer to emit and receive ultrasound signals. The device processes these signals to provide clinical information regarding blood flow or tissue movement. It is intended for use by healthcare professionals in clinical settings. The output is used by clinicians to assess vascular or physiological conditions, aiding in diagnostic decision-making and patient management. ## Clinical Evidence No clinical data provided; clearance based on substantial equivalence and requirement for post-clearance submission of acoustic output measurements. ## Technological Characteristics Diagnostic ultrasound device featuring a 5 MHz transducer. Operates as a Doppler ultrasound system. Subject to 21 CFR 892.1540. Requires compliance with Good Manufacturing Practice (GMP) and Quality System Regulation (21 CFR Part 820). ## Regulatory Identification A nonfetal ultrasonic monitor is a device that projects a continuous high-frequency sound wave into body tissue other than a fetus to determine frequency changes (doppler shift) in the reflected wave and is intended for use in the investigation of nonfetal blood flow and other nonfetal body tissues in motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. ## 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 the text "DEPARTMENT OF HEALTH & HUMAN SERVICES" in a bold, sans-serif font. The text is arranged on a single line and is centered horizontally. The words are capitalized, and the ampersand symbol (&) is used to connect "HEALTH" and "HUMAN". Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 David W. Wagner Director, Quality Assurance and Regulatory Affairs Imex Medical Systems, Inc. 6355 Joyce Drive Golden, Colorado 80403 Re : K973336 IMEX StethoDop™ (Doppler Ultrasound Device) Dated: December 11, 1997 December 17, 1997 Received: Regulatory class: İI 90 JAF 21 CFR 892.1540/Procode: Dear Mr. Wagner: 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 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. You may, therefore, market the device, subject to the general controls The general controls provisions of the Act include provisions Act (Act). requirements for registration, listing of devices, good manufacturing practices, labeling, and prohibitions against misbranding and adulteration. This determination of substantial equivalence applies to the following transducers intended for use with the IMEX StethoDop™, as described in your premarket notification: ## Transducer Model Number 5 MHz 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 Good ……… Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic QS inspections, the FDA will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, the Food and Drug Administration (FDA) may publish further announcements concerning your device in the Federal Register Please note: this response to your premarket notification does not affect any obligation you may have under sections 531 and 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This determination of substantial equivalence is granted on the condition that prior to shipping the first device, you submit a postclearance special report. This report should contain complete information, including acoustic output measurements based on production line devices, requested in Appendix G, (enclosed) of the Center's September 30, 1997 "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers." If the special report is incomplete or contains unacceptable values (e.g., acoustic output greater than approved levels), then the 510(k) clearance may not apply to the production units which as a result may be considered adulterated or misbranded. FEB - 5 1998 {1}------------------------------------------------ ## Page 2 - David W. Waqner The special report should reference the manufacturer's 510(k) number. It should be clearly and prominently marked "ADD-TO-FILE" and should be submitted in duplicate to: > Food and Drug Administration Center for Devices and Radiological Health Document Mail Center (HFZ-401) 9200 Corporate Boulevard Rockville, Maryland 20850 This letter will allow you to begin marketing your device as described in your 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 market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4591. 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 Other general information on your responsibilities under the Act may 807.97). be obtained from the Division of Small Manufacturers Assistance at its tollfree number (800) 638-2041 or at (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". If you have any questions regarding the content of this letter, please contact Paul Gammell at (301) 594-1212. Sincerely yours, Daniel A. Siggman Lillian Yin, Ph.D. Director, Division of Reproductive, Abdominal, Ear, Nose and Throat, nd Radiological Devices ffice of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ K973336 Appendix F ## Indications for Use Form ## Fill out one form for each ultrasound system and each transducer. | | Mode of Operation | | | | | | | | | | |----------------------------------|-------------------|---|---|-----|-----|------------------|------------------|------------------------------|-----------------------|--------------------| | Clinical Application | A | B | M | PWD | CWD | Color
Doppler | Power
Doppler | Color
Velocity
Imaging | Combined
(specify) | Other
(specify) | | Ophthalmic | | | | | | | | | | | | Fetal | | | | | | | | | | | | Abdominal | | | | | | | | | | | | Intra-operative
(specify) | | | | | | | | | | | | Intra-operative
Neurological | | | | | | | | | | | | Pediatric | | | | | | | | | | | | Small Organ (specify) | | | | | | | | | | | | Neonatal Cephalic | | | | | | | | | | | | Adult Cephalic | | | | | | | | | | | | Cardiac | | | | | | | | | | | | Trans-esophageal | | | | | | | | | | | | Trans-Rectal | | | | | | | | | | | | Trans-Vaginal | | | | | | | | | | | | Trans-Urethral | | | | | | | | | | | | Intra-Luminal | | | | | | | | | | | | Peripheral Vascular | | | | | | | | | | | | Laparoscopic | | | | | | | | | | | | Musculo-Skeletal
Conventional | | | | | | | | | | | | Musculo-Skeletal
Superficial | | | | | | | | | | | | Other (specify) | | | | | | | | | | | Additional Comments: IMEX STETHODOP K973336 (PLEASE DO NOT WRITE BELOW THIS LINE . CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Prescription Use (Per 21 CFR 801.109) Division of Reproductive, Abdominal, ENT, and Radiological Devices 510(k) Number: K973336 Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAF/K973336](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/JAF/K973336) **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