LIFEPAK 15 AC Power Adapter (41577-000333)

FDA 510(k) K253099 · Physio-Control, Inc.

Substantially Equivalent

510(k) numberK253099

Submission

Device name
LIFEPAK 15 AC Power Adapter (41577-000333)
Applicant
Physio-Control, Inc.
Redmond, WA, US
Received
September 24, 2025
Decision date
October 14, 2025
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MPD – Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5300
Specialty
Cardiovascular
Life-sustaining
Yes

Other 510(k)s with product code MPD

510(k)DeviceApplicantDecision
K240162LIFEPAK® 35 AC Power Adapter (41335-000001)MPD · Traditional Stryker Physio-Control04/19/2024SE
K062331HIGHPAK-12MPD · Traditional Ad Elektronik GmbH07/10/2007SE

More from Ad Elektronik GmbH

510(k)DeviceDecision
K240156LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV…DSA · Traditional 04/30/2024SE
K182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsLDD · Traditional 06/03/2019SE
K142430LIFEPAK 15 monitor/defibrillatorMKJ · Traditional 12/19/2014SE
K130454Lifepak 20 Defibrillator/Monitor, Lifepak 20E Defibrillator/MonitorMKJ · Traditional 08/21/2013SE
K123597Truecpr Coaching DeviceLIX · Traditional 04/17/2013SE
K122600Lifepak 1000 DefibrillatorMKJ · Traditional 10/11/2012SE
K103567Lifepak 15 Monitor/DefibrillatorMKJ · Traditional 03/22/2011SE
K102972Lifepak 12MKJ · Special 12/22/2010SE
K102757Lifenet SystemMSX · Special 11/05/2010SE
K093925Lifenet SystemMSX · Special 01/12/2010SE

Questions and answers

When was LIFEPAK 15 AC Power Adapter (41577-000333) cleared by the FDA?

LIFEPAK 15 AC Power Adapter (41577-000333) (K253099) received a 510(k) decision of Substantially Equivalent on October 14, 2025, 20 days after the submission was received.

What is the product code of K253099?

The FDA product code is MPD – Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator, a Class II (moderate risk) device regulated under 21 CFR 870.5300.