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FDA 510(k), K800839, MEDESCAN
FDA 510(k), K800839, MEDESCAN
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510(K) Number: K800839
Device Name: MEDESCAN
Manufacturer: MEDEFIELD PTY. LTD.
Device Classification Name: Medium, Contrast, Radiologic
Regulation Number:
Classification Product Code: KTA
Date Received: 04/15/1980
Decision Date: 05/30/1980
Regulation Medical Specialty:
Device Name: MEDESCAN
Manufacturer: MEDEFIELD PTY. LTD.
Device Classification Name: Medium, Contrast, Radiologic
Regulation Number:
Classification Product Code: KTA
Date Received: 04/15/1980
Decision Date: 05/30/1980
Regulation Medical Specialty:
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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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