MPE
- Product code
- MPE
- Device name
- Auxiliary Power Supply (Acor Dc) For External Transcutaneous Cardiac Pacemaker
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5550
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Life-sustaining / life-supporting
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: MPE
Classification and pathway per current FDA publications. Data from openFDA (CC0).