LIFEPAK® 35 AC Power Adapter (41335-000001)
K-Number: K240162 · 2024-04-19
ApplicantStryker Physio-Control
Decision Date2024-04-19
Product CodeMPD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
LIFEPAK® 35 AC Power Adapter (41335-000001) is a medical device manufactured by Stryker Physio-Control. It received FDA 510(k) clearance on 2024-04-19 under approval number K240162. 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® 35 AC Power Adapter (41335-000001)?
LIFEPAK® 35 AC Power Adapter (41335-000001) is a medical device that received FDA 510(k) clearance on 2024-04-19. It is manufactured by Stryker Physio-Control. The 510(k) number is K240162.
When was LIFEPAK® 35 AC Power Adapter (41335-000001) approved by the FDA?
LIFEPAK® 35 AC Power Adapter (41335-000001) received FDA 510(k) clearance on 2024-04-19, under approval number K240162.
What company makes LIFEPAK® 35 AC Power Adapter (41335-000001)?
LIFEPAK® 35 AC Power Adapter (41335-000001) is manufactured by Stryker Physio-Control.
What is the FDA product code for LIFEPAK® 35 AC Power Adapter (41335-000001)?
The FDA product code for LIFEPAK® 35 AC Power Adapter (41335-000001) is MPD.
Other Devices by Stryker Physio-Control
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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.