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FDA 510(k)

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider

K-Number: K172856 · 2017-11-16

ApplicantStryker Sustainability Solutions
Decision Date2017-11-16
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2017-11-16 under approval number K172856. 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 Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider?

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K172856.

When was Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider approved by the FDA?

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider received FDA 510(k) clearance on 2017-11-16, under approval number K172856.

What company makes Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider?

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider?

The FDA product code for Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider is GEI.

Related Clinical Trials

NCT07517783 "Comparison of Clip-Based and Clipless Laparoscopic Gallbladder Surgery in Controlling Bleeding" COMPLETED

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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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