Product code MPD— Cardiovascular
HIGHPAK-12
- Classification name
- Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator
- Device class
- Class 2
- Regulation
- 21 CFR 870.5300
- Advisory panel
- Cardiovascular
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code MPD
FDA has cleared devices under product code MPD between 2007 and 2025, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2025
- 2024
- 2007
Top applicants under product code MPD
Recent clearances under product code MPD
Data sourced from openFDA. This site is unofficial and independent of the FDA.