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FDA 510(k)

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider

K-Number: K162751 · 2017-05-01

Decision Date2017-05-01
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is a medical device manufactured by Surgical Instrument Services and Savings, Inc.. It received FDA 510(k) clearance on 2017-05-01 under approval number K162751. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is a medical device that received FDA 510(k) clearance on 2017-05-01. It is manufactured by Surgical Instrument Services and Savings, Inc.. The 510(k) number is K162751.

When was Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider approved by the FDA?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider received FDA 510(k) clearance on 2017-05-01, under approval number K162751.

What company makes Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is manufactured by Surgical Instrument Services and Savings, Inc..

What is the FDA product code for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?

The FDA product code for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider is NUJ.

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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.