Ultrasonic Pulsed Echo Imaging System RT30
FDA 510(k) K827891 · General Electric Co.
510(k) numberK827891
Submission
- Device name
- Ultrasonic Pulsed Echo Imaging System RT30
- Applicant
- General Electric Co.
Schenectady, NY, US - Received
- August 11, 1982
- Decision date
- September 29, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Ultrasonic Pulsed Echo Imaging System RT30 cleared by the FDA?
Ultrasonic Pulsed Echo Imaging System RT30 (K827891) received a 510(k) decision of Substantially Equivalent on September 29, 1982, 49 days after the submission was received.