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FDA 510(k)

Streamline 6495 Bipolar Temporary Myocardial Pacing Lead

K-Number: K161249 · 2016-08-19

ApplicantMedtronic
Decision Date2016-08-19
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Streamline 6495 Bipolar Temporary Myocardial Pacing Lead is a medical device manufactured by Medtronic. It received FDA 510(k) clearance on 2016-08-19 under approval number K161249. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Streamline 6495 Bipolar Temporary Myocardial Pacing Lead?

Streamline 6495 Bipolar Temporary Myocardial Pacing Lead is a medical device that received FDA 510(k) clearance on 2016-08-19. It is manufactured by Medtronic. The 510(k) number is K161249.

When was Streamline 6495 Bipolar Temporary Myocardial Pacing Lead approved by the FDA?

Streamline 6495 Bipolar Temporary Myocardial Pacing Lead received FDA 510(k) clearance on 2016-08-19, under approval number K161249.

What company makes Streamline 6495 Bipolar Temporary Myocardial Pacing Lead?

Streamline 6495 Bipolar Temporary Myocardial Pacing Lead is manufactured by Medtronic.

What is the FDA product code for Streamline 6495 Bipolar Temporary Myocardial Pacing Lead?

The FDA product code for Streamline 6495 Bipolar Temporary Myocardial Pacing Lead is LDF.

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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.