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FDA 510(k), K092117, SCENAR, MODEL 10
FDA 510(k), K092117, SCENAR, MODEL 10
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510(K) Number: K092117
Device Name: SCENAR, MODEL 10
Manufacturer: RITM OKB ZAO
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 07/14/2009
Decision Date: 05/28/2010
Regulation Medical Specialty:
Device Name: SCENAR, MODEL 10
Manufacturer: RITM OKB ZAO
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 07/14/2009
Decision Date: 05/28/2010
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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