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FDA 510(k)

Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)

K-Number: K220481 · 2022-05-25

ApplicantStryker Sustainability Solutions
Decision Date2022-05-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2022-05-25 under approval number K220481. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)?

Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) is a medical device that received FDA 510(k) clearance on 2022-05-25. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K220481.

When was Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) approved by the FDA?

Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) received FDA 510(k) clearance on 2022-05-25, under approval number K220481.

What company makes Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)?

Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)?

The FDA product code for Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019) is GEI.

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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.

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