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FDA 510(k)

LigaSure Retractable L-Hook Laparoscopic Sealer/Divider

K-Number: K161804 · 2016-09-16

ApplicantCovidien
Decision Date2016-09-16
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LigaSure Retractable L-Hook Laparoscopic Sealer/Divider is a medical device manufactured by Covidien. It received FDA 510(k) clearance on 2016-09-16 under approval number K161804. 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 LigaSure Retractable L-Hook Laparoscopic Sealer/Divider?

LigaSure Retractable L-Hook Laparoscopic Sealer/Divider is a medical device that received FDA 510(k) clearance on 2016-09-16. It is manufactured by Covidien. The 510(k) number is K161804.

When was LigaSure Retractable L-Hook Laparoscopic Sealer/Divider approved by the FDA?

LigaSure Retractable L-Hook Laparoscopic Sealer/Divider received FDA 510(k) clearance on 2016-09-16, under approval number K161804.

What company makes LigaSure Retractable L-Hook Laparoscopic Sealer/Divider?

LigaSure Retractable L-Hook Laparoscopic Sealer/Divider is manufactured by Covidien.

What is the FDA product code for LigaSure Retractable L-Hook Laparoscopic Sealer/Divider?

The FDA product code for LigaSure Retractable L-Hook Laparoscopic Sealer/Divider is GEI.

Related Clinical Trials

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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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