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FDA 510(k)

Reprocessed CS Diagnostic Electrophysiology Catheter

K-Number: K181056 · 2019-01-24

Decision Date2019-01-24
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed CS Diagnostic Electrophysiology Catheter is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2019-01-24 under approval number K181056. The device is classified under product code NLH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed CS Diagnostic Electrophysiology Catheter?

Reprocessed CS Diagnostic Electrophysiology Catheter is a medical device that received FDA 510(k) clearance on 2019-01-24. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K181056.

When was Reprocessed CS Diagnostic Electrophysiology Catheter approved by the FDA?

Reprocessed CS Diagnostic Electrophysiology Catheter received FDA 510(k) clearance on 2019-01-24, under approval number K181056.

What company makes Reprocessed CS Diagnostic Electrophysiology Catheter?

Reprocessed CS Diagnostic Electrophysiology Catheter is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Reprocessed CS Diagnostic Electrophysiology Catheter?

The FDA product code for Reprocessed CS Diagnostic Electrophysiology Catheter is NLH.

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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.