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FDA 510(k), K173085, invendoscopy E210 System
FDA 510(k), K173085, invendoscopy E210 System
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510(K) Number: K173085
Device Name: invendoscopy E210 System
Manufacturer: invendo medical GmbH
Device Classification Name: colonoscope and accessories, flexible/rigid
Regulation Number: 876.1500
Classification Product Code: FDF
Date Received: 09/29/2017
Decision Date: 01/08/2018
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: invendoscopy E210 System
Manufacturer: invendo medical GmbH
Device Classification Name: colonoscope and accessories, flexible/rigid
Regulation Number: 876.1500
Classification Product Code: FDF
Date Received: 09/29/2017
Decision Date: 01/08/2018
Regulation Medical Specialty: Gastroenterology/Urology
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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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