Equidyne Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Equidyne Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Equidyne Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Historical record: 5 cleared submissions from 1995 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Equidyne Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Equidyne Systems, Inc.
5 devices
Cleared
Sep 05, 2002
INJEX 30 NEEDLE FREE INJECTION SYSTEM, MODEL 100000
General Hospital
38d
Cleared
Jul 23, 2002
INJEX 30 NEEDLE FREE INJECTION SYSTEM
General Hospital
21d
Cleared
Jun 01, 2001
JET SYRINGE MODEL-100500
General Hospital
179d
Cleared
Mar 06, 2001
INJEX 50 SYSTEM
General Hospital
83d
Cleared
Aug 18, 1995
HYPEX(TM) JET INJECTOR
General Hospital
260d