Portable Power Systems, Inc.
Portable Power Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1997.
Top product codes for Portable Power Systems, Inc.
Recent clearances by Portable Power Systems, Inc.
- K970234 — SEALED LEAD ACID BATTERY PACK
- K946080 — PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATOR
- K945043 — BATTERY PACK #PMX120-18A
- K931348 — BATTERY PACK #1005NC
- K931483 — REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.
- K931484 — REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S
- K932823 — BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK
- K933065 — BATTERY PACK# S1009LA
- K934015 — RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB
- K934439 — RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITOR
- K934508 — BATTERY PACK# S1024NC
- K931716 — BATTERY PACK 1017LA
- K931266 — BATTERY PACK #1012NC
- K925674 — BATTERY PACK #1014NC
- K925675 — BATTERY PACK #1015NC
- K925449 — REPLACEMENT RECHARGEABLE BATTERY PACK'S
- K924798 — BATTERY PACK
- K923864 — BATTERY PACK
Data sourced from openFDA. This site is unofficial and independent of the FDA.