Arrow Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow Intl., Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARROWGARD EVOLUTION ANTIMICROBIAL PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) MODEL: S-44041-002, S-45041-002, S-45504, ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520, ARROW INTERNATIONAL, INC., SURGICAL DRAPES
110
Total
105
Cleared
0
Denied
Arrow Intl., Inc. has 105 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 105 cleared submissions from 1976 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arrow Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow Intl., Inc.
110 devices
Cleared
Aug 27, 2010
ARROWGARD EVOLUTION ANTIMICROBIAL PERIPHERALLY INSERTED CENTRAL CATHETER...
General Hospital
175d
Cleared
Dec 18, 2009
ARROW SELDINGER ARTERIAL CATHERIZATION DEVICES, MODELS EX SAC 00520
Cardiovascular
79d
Cleared
Oct 10, 2007
ARROW INTERNATIONAL, INC., SURGICAL DRAPES
General Hospital
133d
Cleared
Sep 26, 2007
ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT
General Hospital
65d
Cleared
Jul 17, 2007
NON-ABSORBABLE SILK SUTURE
General & Plastic Surgery
88d
Cleared
Apr 06, 2006
AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES
Cardiovascular
58d
Cleared
Aug 27, 2004
PICC
General Hospital
21d
Cleared
Jul 12, 2004
SHARPSAWAY II LOCKING DISPOSABLE CUP
General Hospital
70d
Cleared
May 06, 2004
INTRA-AORTIC BALLOON (IAB)
Cardiovascular
38d
Cleared
Apr 28, 2004
HEMOSONIC 200HEMODYNAMIC MONITOR
Toxicology
30d
Cleared
Mar 01, 2004
ARROW ECHOGENIC INTRODUCER NEEDLE
Cardiovascular
41d
Cleared
Nov 25, 2003
MONITOR, MODEL HSM-00200
Cardiovascular
228d
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