Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider
K-Number: K162751 · 2017-05-01
Device Summary
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. The listed applicant is Surgical Instrument Services and Savings, Inc.. The 510(k) number is K162751.
When did Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider receive FDA 510(k) clearance?
Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider received FDA 510(k) clearance on 2017-05-01, under 510(k) number K162751.
Who is the listed applicant for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider?
The FDA 510(k) record lists Surgical Instrument Services and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Surgical Instrument Services and Savings, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NUJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.