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FDA 510(k)

LIFEPAK 15 AC Power Adapter (41577-000333)

K-Number: K253099 · 2025-10-14

ApplicantPhysio-Control, Inc.
Decision Date2025-10-14
Product CodeMPD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEPAK 15 AC Power Adapter (41577-000333) is a medical device manufactured by Physio-Control, Inc.. It received FDA 510(k) clearance on 2025-10-14 under approval number K253099. The device is classified under product code MPD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPAK 15 AC Power Adapter (41577-000333)?

LIFEPAK 15 AC Power Adapter (41577-000333) is a medical device that received FDA 510(k) clearance on 2025-10-14. It is manufactured by Physio-Control, Inc.. The 510(k) number is K253099.

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

LIFEPAK 15 AC Power Adapter (41577-000333) received FDA 510(k) clearance on 2025-10-14, under approval number K253099.

What company makes LIFEPAK 15 AC Power Adapter (41577-000333)?

LIFEPAK 15 AC Power Adapter (41577-000333) is manufactured by Physio-Control, Inc..

What is the FDA product code for LIFEPAK 15 AC Power Adapter (41577-000333)?

The FDA product code for LIFEPAK 15 AC Power Adapter (41577-000333) is MPD.

Other Devices by Physio-Control, Inc.

K182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors K240156LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024) PMA P160012Automated external defibrillators (non-wearable) PMA P170018Automated external defibrillators (non-wearable) PMA P160026Automated external defibrillators (non-wearable)

Related Devices (Code: MPD)

K240162LIFEPAK® 35 AC Power Adapter (41335-000001)Stryker Physio-Control

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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