Distronic Sterile Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Distronic Sterile Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Distronic Sterile Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Portsmouth, US.
Historical record: 8 cleared submissions from 1995 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Distronic Sterile Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Distronic Sterile Products, Inc.
8 devices
Cleared
Feb 21, 1996
WINGED & SUBCUTANEOUS INFUSION SETS
General Hospital
65d
Cleared
Feb 21, 1996
VENTED SOLUTION SET
General Hospital
64d
Cleared
Jan 23, 1996
EXTENSION SET WITH CHECK VALVE
General Hospital
84d
Cleared
Jan 23, 1996
MINIBORE STOPCOCK SET
General Hospital
84d
Cleared
Aug 07, 1995
SOLUTION ADMINISTRATION SET
General Hospital
56d
Cleared
Jul 26, 1995
CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE
General Hospital
167d
Cleared
Jul 14, 1995
60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2...
General Hospital
32d
Cleared
Feb 08, 1995
INTRAVASCULAR ADMINISTRATION SET
General Hospital
107d