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FDA 510(k), K031018, AUTOGEL PAD
FDA 510(k), K031018, AUTOGEL PAD
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510(K) Number: K031018
Device Name: AUTOGEL PAD
Manufacturer: RICH-MAR CORP.
Device Classification Name: media, coupling, ultrasound
Regulation Number: 892.1570
Classification Product Code: MUI
Date Received: 03/31/2003
Decision Date: 12/08/2003
Regulation Medical Specialty: Radiology
Device Name: AUTOGEL PAD
Manufacturer: RICH-MAR CORP.
Device Classification Name: media, coupling, ultrasound
Regulation Number: 892.1570
Classification Product Code: MUI
Date Received: 03/31/2003
Decision Date: 12/08/2003
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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