Atlas FDA

LIFEPAK 15 AC Power Adapter (41577-000333)

FDA 510(k) clearance K253099 · decided 2025-10-14

Clearance details

K-number
K253099
Device name
LIFEPAK 15 AC Power Adapter (41577-000333)
Applicant
Physio-Control, Inc.
Decision
Substantially Equivalent
Date received
2025-09-24
Decision date
2025-10-14
Days to decision
20 days
Clearance type
Special
Product code
MPD
Device class
2
Regulation number
870.5300
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Redmond, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LIFEPAK® 35 AC Power Adapter (41335-000001) (K240162)Stryker Physio-Control2024-04-19
HIGHPAK-12 (K062331)Ad Elektronik GmbH2007-07-10

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
LIFEPAK® 35 monitor/defibrillator (P160026/S071)Physio-Control, Inc.2026-08-06
LIFEPAK® CR2 Defibrillator (P170018/S025)Physio-Control, Inc.2026-07-30
LIFEPAK 1000 DEFIBRILLATOR, LIFEPAK 20 DEFIBRILLATOR/ MONITOR, LIFEPAK 20E DEFIBRILLATOR/ MONITOR, LIFEPAK 15 MONITOR/DE (P160026/S070)Physio-Control, Inc.2026-07-30
LIFEPAK® 15 monitor/defibrillator (P160026/S068)Physio-Control, Inc.2026-06-25
LIFEPAK® 15 monitor/defibrillator (P160026/S067)Physio-Control, Inc.2026-05-06
LIFEPAK 35 monitor/defibrillator (P160026/S066)Physio-Control, Inc.2026-03-05
LIFEPAK® 35 monitor/defibrillator (P160026/S065)Physio-Control, Inc.2026-02-23
LIFEPAK® 35 Defibrillator/monitor (P160026/S063)Physio-Control, Inc.2025-12-04