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FDA 510(k)

REPROCESSED VESSEL SEALER

K-Number: K123096 · 2013-01-25

ApplicantSterilmed, Inc.
Decision Date2013-01-25
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED VESSEL SEALER is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2013-01-25 under 510(k) number K123096. 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 REPROCESSED VESSEL SEALER?

REPROCESSED VESSEL SEALER is a medical device that received FDA 510(k) clearance on 2013-01-25. The listed applicant is Sterilmed, Inc.. The 510(k) number is K123096.

When did REPROCESSED VESSEL SEALER receive FDA 510(k) clearance?

REPROCESSED VESSEL SEALER received FDA 510(k) clearance on 2013-01-25, under 510(k) number K123096.

Who is the listed applicant for REPROCESSED VESSEL SEALER?

The FDA 510(k) record lists Sterilmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED VESSEL SEALER?

The FDA product code for REPROCESSED VESSEL SEALER is NUJ.

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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.

K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)Surgical Instrument Service and Savings, Inc.K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLCK182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren

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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