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FDA 510(k), K073323, SA-3000P
FDA 510(k), K073323, SA-3000P
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510(K) Number: K073323
Device Name: SA-3000P
Manufacturer: YOO BYUNG-KUK
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: JOM
Classification Product Code: 11/27/2007
Date Received: 11/29/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: SA-3000P
Manufacturer: YOO BYUNG-KUK
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: JOM
Classification Product Code: 11/27/2007
Date Received: 11/29/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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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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