FDA 510(k), K182870, Introcan Safety 3 Closed IV Catheter
FDA 510(k), K182870, Introcan Safety 3 Closed IV Catheter
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510(K) Number: K182870
Device Name: Introcan Safety 3 Closed IV Catheter
Manufacturer: Tracy Larish
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 10/12/2018
Date Received: 03/07/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: Introcan Safety 3 Closed IV Catheter
Manufacturer: Tracy Larish
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: 10/12/2018
Date Received: 03/07/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
- 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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