The following data is part of a premarket notification filed by Mps Acacia with the FDA for Mps Acacia Pain Kit.
| Device ID | K003476 |
| 510k Number | K003476 |
| Device Name: | MPS ACACIA PAIN KIT |
| Classification | Pump, Infusion, Elastomeric |
| Applicant | MPS ACACIA 499 NIBUS ST., SUITE E Brea, CA 92821 |
| Contact | Fergie F Ferguson |
| Correspondent | Fergie F Ferguson MPS ACACIA 499 NIBUS ST., SUITE E Brea, CA 92821 |
| Product Code | MEB |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-11-09 |
| Decision Date | 2001-01-12 |