FDA 510(k)

LIFEPAK® 35 AC Power Adapter (41335-000001)

K-Number: K240162 · 2024-04-19

Decision Date2024-04-19

Product CodeMPD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

LIFEPAK® 35 AC Power Adapter (41335-000001) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Physio-Control. It received FDA 510(k) clearance on 2024-04-19 under 510(k) 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. The listed applicant is Stryker Physio-Control. The 510(k) number is K240162.

When did LIFEPAK® 35 AC Power Adapter (41335-000001) receive FDA 510(k) clearance?

LIFEPAK® 35 AC Power Adapter (41335-000001) received FDA 510(k) clearance on 2024-04-19, under 510(k) number K240162.

Who is the listed applicant for LIFEPAK® 35 AC Power Adapter (41335-000001)?

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

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 records listing Stryker Physio-Control 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.

K240377LIFEPAK® ECG Cables

Related Devices (Code: MPD)

K253099LIFEPAK 15 AC Power Adapter (41577-000333)Physio-Control, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.