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FDA 510(k), K163358, Introcan Safety 3 Closed IV Catheter
FDA 510(k), K163358, Introcan Safety 3 Closed IV Catheter
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510(K) Number: K163358
Device Name: Introcan Safety 3 Closed IV Catheter
Manufacturer: B.BRAUN MELSUNGEN AG
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 11/30/2016
Decision Date: 04/28/2017
Regulation Medical Specialty: General Hospital
Device Name: Introcan Safety 3 Closed IV Catheter
Manufacturer: B.BRAUN MELSUNGEN AG
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 11/30/2016
Decision Date: 04/28/2017
Regulation Medical Specialty: General Hospital
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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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