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FDA 510(k)

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars

K-Number: K153258 · 2016-04-05

Decision Date2016-04-05
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Service and Savings (Dba Medline Renewal. It received FDA 510(k) clearance on 2016-04-05 under 510(k) number K153258. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is a medical device that received FDA 510(k) clearance on 2016-04-05. The listed applicant is Surgical Instrument Service and Savings (Dba Medline Renewal. The 510(k) number is K153258.

When did Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars received FDA 510(k) clearance on 2016-04-05, under 510(k) number K153258.

Who is the listed applicant for Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

The FDA 510(k) record lists Surgical Instrument Service and Savings (Dba Medline Renewal as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

The FDA product code for Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is NLM.

Related Devices (Code: NLM)

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

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