# Portable Power Systems, Inc.

- Location (FDA's records): Castle Rock, CO
- FDA decisions: 18 (1992–1997): 18 510(k) clearances
- Product codes: IZL (4), LDD (4), DPS (2), FLL (2), FRN (1), DSI (1), BTA (1), DXN (1), FCO (1), BZD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K970234: Sealed Lead Acid Battery Pack (May 2, 1997)
- K946080: Physio Control Lifepak 200 Auto Defibrillator (Aug 2, 1995)
- K945043: Battery Pack #PMX120-18A (Jan 20, 1995)
- K934439: Rechargeable Battery Pack for Critikon 8100 Vital Signs Monitor (Feb 17, 1994)
- K931483: Replacement Batery for GE Amx-4 Port. X-Ray Mach. (Feb 17, 1994)
- K933065: Battery Pack# S1009LA (Feb 17, 1994)
- K934508: Battery Pack# S1024NC (Feb 17, 1994)
- K934015: Recharge Replace Battery PK Spacelabs 4045 Mon/Defib (Feb 17, 1994)

Source page: https://510kreport.com/company/portable-power-systems