Acuson S519B Transducer
FDA 510(k) K863236 · Acuson Computed Sonography
510(k) numberK863236
Submission
- Device name
- Acuson S519B Transducer
- Applicant
- Acuson Computed Sonography
Mountain View, CA, US - Received
- August 21, 1986
- Decision date
- February 13, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Acuson Computed Sonography
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|---|---|---|
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| K871506 | Acuson L538 TransducerJOP · Traditional | 09/28/1987SE |
| K871416 | Auxiliary Continuous Wave Doppler TransducerJOP · Traditional | 09/28/1987SE |
| K871239 | Acuson Physiological Control ModuleDPS · Traditional | 06/05/1987SE |
| K864578 | Acuson TV519 TransducerHGL · Traditional | 03/27/1987SE |
Questions and answers
When was Acuson S519B Transducer cleared by the FDA?
Acuson S519B Transducer (K863236) received a 510(k) decision of Substantially Equivalent on February 13, 1987, 176 days after the submission was received.