510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MPDClass II

Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator

21 CFR 870.5300 / Cardiovascular
FDA source (opens on fda.gov)

MPD is the FDA product code for Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator, a class II device type, regulated under 21 CFR 870.5300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MPD
Device name
Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator
Regulation
21 CFR 870.5300
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code MPD

By decision year
3 clearances under product code MPD with a decision year between 2007 and 2025, 2007 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MPD by decision year
YearClearances
20071
20241
20251

Applicants with the most clearances

Product code MPD
Applicants holding the most 510(k) clearances under product code MPD
ApplicantClearances
Ad Elektronik GmbH1
Physio Control, Inc.1
Stryker Physio-Control1

Companies listing this code with FDA

Companies whose registered establishments list this code