FDA product code MPD: Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator
MPD is the FDA product code for auxiliary power supply (ac or dc) for low-energy dc-defibrillator. It is a Class II device, regulated under 21 CFR 870.5300 and reviewed by the Cardiovascular panel. FDA has cleared 3 510(k) submissions under MPD, 2 in the last five years, from 3 different applicants. The average 510(k) review took 147 days (median 88); 54 days on average over the last three years.
Classification
| Field | Value |
|---|---|
| Device name | Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator |
| Device class | Class II |
| Regulation | 21 CFR 870.5300 |
| Review panel | CV — Cardiovascular |
| Medical specialty | Cardiovascular |
| Premarket route | 510(k) |
| Life-sustaining or supporting | Yes |
510(k) clearances per year for MPD
| Year | Clearances | Avg. review days |
|---|---|---|
| 2024 | 1 | 88 |
| 2025 | 1 | 20 |
Compare with all 510(k) review times · Search every MPD clearance
Top MPD applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Physio-Control, Inc. | 1 | 2025-10-14 |
| Stryker Physio-Control | 1 | 2024-04-19 |
| Ad Elektronik GmbH | 1 | 2007-07-10 |
Most recent MPD clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K253099 | Physio-Control, Inc. | LIFEPAK 15 AC Power Adapter (41577-000333) | 2025-10-14 | 20 |
| K240162 | Stryker Physio-Control | LIFEPAK® 35 AC Power Adapter (41335-000001) | 2024-04-19 | 88 |
| K062331 | Ad Elektronik GmbH | HIGHPAK-12 | 2007-07-10 | 334 |
Recalls for MPD devices
openFDA lists no recalls for product code MPD.
Frequently asked questions
What is FDA product code MPD?
MPD is the FDA product code for auxiliary power supply (ac or dc) for low-energy dc-defibrillator. It is a Class II device, regulated under 21 CFR 870.5300 and reviewed by the Cardiovascular panel.
What device class is MPD?
Class II, regulation 21 CFR 870.5300. Typical premarket route: 510(k).
How long does a 510(k) take for product code MPD?
Across 3 cleared submissions the average was 147 days from receipt to decision (median 88).
Which companies have the most MPD clearances?
Physio-Control, Inc. (1); Stryker Physio-Control (1); Ad Elektronik GmbH (1).
Next steps
- Run an FDA pathway report with predicate devices for product code MPD
- Run a recall and safety report across every MPD manufacturer
- Watch product code MPD for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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