Atlas FDA

LIFEPAK® 15 monitor/defibrillator

FDA premarket approval P160026/S043 · decided 2023-10-18

Approval details

PMA number
P160026
Supplement
S043
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
LIFEPAK® 15 monitor/defibrillator
Generic name
Automated external defibrillators (non-wearable)
Applicant
Physio-Control, Inc.
Date received
2023-09-28
Decision date
2023-10-18
Days to decision
20 days
Decision code
APPR
Product code
MKJ
Advisory committee
Cardiovascular
Expedited review
No
Location
Redmond, WA
Statement
approval for a new warning associated with leaving the LIFEPAK 15 device powered on for an extended amount of time. Additionally, an existing warning associated with the AED Mode will be updated to include clarifying information.

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510(k) clearances by this applicant

RecordFirmDate
LIFEPAK 15 AC Power Adapter (41577-000333) (K253099)Physio-Control, Inc.2025-10-14
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) (K240156)Physio-Control, Inc.2024-04-30
Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors (K182503)Physio-Control, Inc.2019-06-03
LIFEPAK 15 monitor/defibrillator (K142430)Physio-Control, Inc.2014-12-19
LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR (K130454)Physio-Control, Inc.2013-08-21
TRUECPR COACHING DEVICE (K123597)Physio-Control, Inc.2013-04-17
LIFEPAK 1000 DEFIBRILLATOR (K122600)Physio-Control, Inc.2012-10-11
LIFEPAK 15 MONITOR/DEFIBRILLATOR (K103567)Physio-Control, Inc.2011-03-22