Solopak Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solopak Medical Products, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Solopak Medical Products, Inc. has 4 FDA 510(k) cleared medical devices. Based in Libertyville, US.
Historical record: 4 cleared submissions from 1996 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Solopak Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solopak Medical Products, Inc.
4 devices
Cleared
Apr 02, 1997
MAXCESS NEEDLEFREE - Y- SITE (100713)
General Hospital
29d
Cleared
Oct 04, 1996
SOLOPAK SIDEKICK INFUSION PUMP AND ADMINISTATION SET
General Hospital
88d
Cleared
Oct 04, 1996
SOLOPAK PARAGON INFUSOR PUMP AND INFUSION SET
General Hospital
39d
Cleared
Mar 21, 1996
MAXCESS NEEDLE FREE CONNECTOR (8200)
General Hospital
34d