Portable Power Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Portable Power Systems, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Portable Power Systems, Inc. has 18 FDA 510(k) cleared medical devices. Based in Castle Rock, US.
Historical record: 18 cleared submissions from 1992 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Portable Power Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Portable Power Systems, Inc.
18 devices
Cleared
May 02, 1997
SEALED LEAD ACID BATTERY PACK
Radiology
101d
Cleared
Aug 02, 1995
PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATOR
Gastroenterology & Urology
232d
Cleared
Jan 20, 1995
BATTERY PACK #PMX120-18A
Radiology
98d
Cleared
Feb 17, 1994
BATTERY PACK #1005NC
General & Plastic Surgery
337d
Cleared
Feb 17, 1994
REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.
Radiology
330d
Cleared
Feb 17, 1994
REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S
Anesthesiology
330d
Cleared
Feb 17, 1994
BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK
Cardiovascular
253d
Cleared
Feb 17, 1994
BATTERY PACK# S1009LA
Cardiovascular
240d
Cleared
Feb 17, 1994
RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB
Cardiovascular
184d
Cleared
Feb 17, 1994
RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITOR
Cardiovascular
178d
Cleared
Feb 17, 1994
BATTERY PACK# S1024NC
Cardiovascular
156d
Cleared
Feb 07, 1994
BATTERY PACK 1017LA
Cardiovascular
307d