Doppler Imaging Option
FDA 510(k) K840140 · Hewlett-Packard Co.
510(k) numberK840140
Submission
- Device name
- Doppler Imaging Option
- Applicant
- Hewlett-Packard Co.
Walker, MI, US - Received
- January 4, 1984
- Decision date
- August 23, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Doppler Imaging Option cleared by the FDA?
Doppler Imaging Option (K840140) received a 510(k) decision of Substantially Equivalent on August 23, 1984, 232 days after the submission was received.
What is the product code of K840140?
The FDA product code is IYN – System, Imaging, Pulsed Doppler, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 892.1550.