Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars
K-Number: K153258 · 2016-04-05
Device Summary
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. It is manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal. The 510(k) number is K153258.
When was Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars approved by the FDA?
Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars received FDA 510(k) clearance on 2016-04-05, under approval number K153258.
What company makes Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?
Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal.
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)
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.