Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
K-Number: K220411 · 2022-05-13
Device Summary
Frequently Asked Questions
What is the Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?
Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is a medical device that received FDA 510(k) clearance on 2022-05-13. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K220411.
When was Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) approved by the FDA?
Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) received FDA 510(k) clearance on 2022-05-13, under approval number K220411.
What company makes Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?
Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is manufactured by Stryker Sustainability Solutions.
What is the FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?
The FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is NUJ.
Other Devices by Stryker Sustainability Solutions
Related Devices (Code: NUJ)
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.