invendoscopy E210 System
K-Number: K173085 · 2018-01-08
ApplicantInvendo Medical GmbH
Decision Date2018-01-08
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
invendoscopy E210 System is a medical device manufactured by Invendo Medical GmbH. It received FDA 510(k) clearance on 2018-01-08 under approval number K173085. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the invendoscopy E210 System?
invendoscopy E210 System is a medical device that received FDA 510(k) clearance on 2018-01-08. It is manufactured by Invendo Medical GmbH. The 510(k) number is K173085.
When was invendoscopy E210 System approved by the FDA?
invendoscopy E210 System received FDA 510(k) clearance on 2018-01-08, under approval number K173085.
What company makes invendoscopy E210 System?
invendoscopy E210 System is manufactured by Invendo Medical GmbH.
What is the FDA product code for invendoscopy E210 System?
The FDA product code for invendoscopy E210 System is FDF.
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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.