FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LIFEPAK 15 AC Power Adapter (41577-000333)

K Number: K253099 · Decision Oct 14, 2025
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
2
Applicant Total
14
Review Days
20

Basic Information

Device Name
LIFEPAK 15 AC Power Adapter (41577-000333)
K Number
K253099
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Physio-Control, Inc.
Date Received
September 24, 2025
Decision Date
October 14, 2025
Product Code
MPD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MPD Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MPD), ordered by most recent decision date.

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Other Clearances by Physio-Control, Inc.

K Number Device Name
K240156 LIFEPAK® 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)
K182503 Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors
K142430 LIFEPAK 15 monitor/defibrillator
K130454 LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR
K123597 TRUECPR COACHING DEVICE
K122600 LIFEPAK 1000 DEFIBRILLATOR
K103567 LIFEPAK 15 MONITOR/DEFIBRILLATOR
K102972 LIFEPAK 12
K102757 LIFENET SYSTEM
K093925 LIFENET SYSTEM
Search all 14 clearances from Physio-Control, Inc. →