The following data is part of a premarket notification filed by Portable Power Systems, Inc. with the FDA for Battery Pack.
| Device ID | K923864 |
| 510k Number | K923864 |
| Device Name: | BATTERY PACK |
| Classification | Dc-defibrillator, Low-energy, (including Paddles) |
| Applicant | PORTABLE POWER SYSTEMS, INC. 1940 TEE LN. Castle Rock, CO 80104 |
| Contact | Norman A Premo |
| Correspondent | Norman A Premo PORTABLE POWER SYSTEMS, INC. 1940 TEE LN. Castle Rock, CO 80104 |
| Product Code | LDD |
| CFR Regulation Number | 870.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-03 |
| Decision Date | 1992-10-05 |