FDA 510(k)

LIFEPAK® ECG Cables

K-Number: K240377 · 2024-05-07

Decision Date2024-05-07

Product CodeDSA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

LIFEPAK® ECG Cables 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 2024-05-07 under 510(k) number K240377. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPAK® ECG Cables?

LIFEPAK® ECG Cables is a medical device that received FDA 510(k) clearance on 2024-05-07. The listed applicant is Stryker Physio-Control. The 510(k) number is K240377.

When did LIFEPAK® ECG Cables receive FDA 510(k) clearance?

LIFEPAK® ECG Cables received FDA 510(k) clearance on 2024-05-07, under 510(k) number K240377.

Who is the listed applicant for LIFEPAK® ECG Cables?

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® ECG Cables?

The FDA product code for LIFEPAK® ECG Cables is DSA.

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.

K240162LIFEPAK® 35 AC Power Adapter (41335-000001)

Related Devices (Code: DSA)

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.