FDA 510(k) Applications Submitted by ANGELA J CARAVELLA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K102194	08/04/2010	SOLCART B	B. BRAUN AVITUM AG
K100334	02/05/2010	DIACAP POLYSULFONE HIFLO 23 HEMODILAYZER , MODEL 72036811	B. BRAUN AVITUM AG
K090884	03/31/2009	PERIFIX ONE PEDIATRIC CATHETER, 20 GA. & 24 GA.	B. BRAUN MEDICAL, INC.
K090905	04/01/2009	ADDEASE 20MM BINARY CONNECTOR WITH 17 GA. NEEDLE	B. BRAUN MEDICAL, INC.
K140838	04/02/2014	IV ADMINISTRATION SET WITH HAND PUMP	B. BRAUN MEDICAL, INC.
K111236	05/02/2011	INTROCAN SAFETY (R) 3 CLOSED IV CATHETER 18GA X 1-3/4 (45MM) AND 18GA X 1-1/4 (32MM) / 20GA X 1-1/4 (32MM) / 20GA X 1	B. BRAUN MELSUNGEN AG
K112636	09/09/2011	CYTOGUARD(TM) CLOSED LUER CONNECTOR	B. BRAUN MEDICAL, INC.
K143082	10/27/2014	IV Administration Sets with 200(micro)m Blood Filter	B. Braun Medical Inc.
K170897	03/27/2017	Surecan Safety II Needle, Surecan Safety II Needle, Surecan Safety II Needle with Caresite Luer Access Device and Y site	B. Braun Medical Inc.
K201469	06/03/2020	Mini Spike Plus 6/8R	B. Braun Medical Inc.
K191658	06/21/2019	IV Sets not made with PVC	B. Braun Medical Inc.