B.Braun Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Introcan Safety® Deep Access XL IV Catheter, Infusomat® Space Volumetric Infusion Pump Administration Sets, VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System
149
Total
146
Cleared
0
Denied
FDA 510(k) Regulatory Record - B.Braun Medical, Inc. General Hospital ✕
80 devices
Cleared
May 15, 2026
Introcan Safety® Deep Access XL IV Catheter
General Hospital
228d
Cleared
Jul 24, 2025
Infusomat® Space Volumetric Infusion Pump Administration Sets
General Hospital
266d
Cleared
Jul 26, 2024
Introcan Safety® 2 IV Catheter
General Hospital
30d
Cleared
Jul 13, 2024
Omnifix Syringe NRFit
General Hospital
59d
Cleared
Jun 23, 2022
Introcan Safety 2 IV Catheter
General Hospital
100d
Cleared
May 14, 2022
Introcan Safety IV Catheter
General Hospital
71d
Cleared
Mar 03, 2022
IV Administration Set
General Hospital
90d
Cleared
Feb 11, 2022
B. Braun Introcan Safety 2 IV Catheter
General Hospital
81d
Cleared
Jan 18, 2022
Microvolume Luer Access Device
General Hospital
133d
Cleared
Oct 25, 2021
Introcan Safety 3 Closed IV Catheter
General Hospital
31d
Cleared
Sep 24, 2021
IV Administration Sets
General Hospital
379d
Cleared
Dec 09, 2020
Mini Spike Plus 6/8R
General Hospital
189d
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