Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control, Inc.. It received FDA 510(k) clearance on 2025-10-14 under 510(k) 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. The listed applicant is Physio-Control, Inc.. The 510(k) number is K253099.

When did LIFEPAK 15 AC Power Adapter (41577-000333) receive FDA 510(k) clearance?

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

Who is the listed applicant for LIFEPAK 15 AC Power Adapter (41577-000333)?

The FDA 510(k) record lists Physio-Control, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 records listing Physio-Control, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

PMA P160026Automated external defibrillators (non-wearable)PMA P170018Automated external defibrillators (non-wearable)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)K182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors

Related Devices (Code: MPD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑