Maestro Digital Video System
FDA 510(k) K920373 · International Imaging Electronics
510(k) numberK920373
Submission
- Device name
- Maestro Digital Video System
- Applicant
- International Imaging Electronics
Addison, IL, US - Received
- January 29, 1992
- Decision date
- June 24, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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Questions and answers
When was Maestro Digital Video System cleared by the FDA?
Maestro Digital Video System (K920373) received a 510(k) decision of Substantially Equivalent on June 24, 1992, 147 days after the submission was received.
What is the product code of K920373?
The FDA product code is IYO – System, Imaging, Pulsed Echo, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 892.1560.