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FDA 510(k), K002533, TCD 100M, PWD13 TRANSDUCER
FDA 510(k), K002533, TCD 100M, PWD13 TRANSDUCER
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510(K) Number: K002533
Device Name: TCD 100M, PWD13 TRANSDUCER
Manufacturer: SPENCER TECHNOLOGIES
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 08/16/2000
Decision Date: 08/30/2000
Regulation Medical Specialty: Radiology
Device Name: TCD 100M, PWD13 TRANSDUCER
Manufacturer: SPENCER TECHNOLOGIES
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 08/16/2000
Decision Date: 08/30/2000
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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