Excelsior Medical Corp. is one of 20324 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Excelsior Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: SWABCAP AND SWABFLUSH, SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311, SWABCAP
9
Total
9
Cleared
0
Denied
Excelsior Medical Corp. has 9 FDA 510(k) cleared medical devices. Based in Long Branch, US.
Historical record: 9 cleared submissions from 1995 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Excelsior Medical Corp. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Excelsior Medical Corp.
9 devices
Cleared
CT
Dec 24, 2013
SWABCAP AND SWABFLUSH
General & Plastic Surgery
260d
Cleared
Feb 10, 2011
SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311
General Hospital
280d
Cleared
Apr 28, 2009
SWABCAP
General Hospital
153d
Cleared
Dec 18, 2008
STERILE FIELD SALINE PRE-FILLED SYRINGE(S)
General Hospital
83d
Cleared
Feb 23, 2007
SYREX HEPARIN LOCK FLUSH SYRINGE, 1 UNIT/ML & 2 UNITS/ML
General Hospital
268d
Cleared
Dec 09, 2005
STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES
General Hospital
32d
Cleared
May 13, 2003
SYREX PRE-FILLED SYRINGE
General Hospital
187d
Cleared
Oct 25, 1996
EXCELSIOR DISPOSABLE SYRINGE W/NORMAL SALINE (.9% SODIUM CHLORIDE)
General Hospital
88d
Cleared
Feb 08, 1995
MICROBORE EXTENSION SET
General Hospital
267d