LIFEPAK® ECG Cables
K-Number: K240377 · 2024-05-07
ApplicantStryker Physio-Control
Decision Date2024-05-07
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
LIFEPAK® ECG Cables is a medical device manufactured by Stryker Physio-Control. It received FDA 510(k) clearance on 2024-05-07 under approval 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. It is manufactured by Stryker Physio-Control. The 510(k) number is K240377.
When was LIFEPAK® ECG Cables approved by the FDA?
LIFEPAK® ECG Cables received FDA 510(k) clearance on 2024-05-07, under approval number K240377.
What company makes LIFEPAK® ECG Cables?
LIFEPAK® ECG Cables is manufactured by Stryker Physio-Control.
What is the FDA product code for LIFEPAK® ECG Cables?
The FDA product code for LIFEPAK® ECG Cables is DSA.
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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.