FTRD System Set
K-Number: K170867 · 2017-07-25
ApplicantOvesco Endoscopy AG
Decision Date2017-07-25
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
FTRD System Set is a medical device manufactured by Ovesco Endoscopy AG. It received FDA 510(k) clearance on 2017-07-25 under approval number K170867. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FTRD System Set?
FTRD System Set is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Ovesco Endoscopy AG. The 510(k) number is K170867.
When was FTRD System Set approved by the FDA?
FTRD System Set received FDA 510(k) clearance on 2017-07-25, under approval number K170867.
What company makes FTRD System Set?
FTRD System Set is manufactured by Ovesco Endoscopy AG.
What is the FDA product code for FTRD System Set?
The FDA product code for FTRD System Set is PKL.
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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.