Cedic Enteral ENFit Transition Connectors
K-Number: K162254 · 2017-05-04
ApplicantCedic S.R.L.
Decision Date2017-05-04
Product CodePIO
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Cedic Enteral ENFit Transition Connectors is a medical device manufactured by Cedic S.R.L.. It received FDA 510(k) clearance on 2017-05-04 under approval number K162254. The device is classified under product code PIO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Cedic Enteral ENFit Transition Connectors?
Cedic Enteral ENFit Transition Connectors is a medical device that received FDA 510(k) clearance on 2017-05-04. It is manufactured by Cedic S.R.L.. The 510(k) number is K162254.
When was Cedic Enteral ENFit Transition Connectors approved by the FDA?
Cedic Enteral ENFit Transition Connectors received FDA 510(k) clearance on 2017-05-04, under approval number K162254.
What company makes Cedic Enteral ENFit Transition Connectors?
Cedic Enteral ENFit Transition Connectors is manufactured by Cedic S.R.L..
What is the FDA product code for Cedic Enteral ENFit Transition Connectors?
The FDA product code for Cedic Enteral ENFit Transition Connectors is PIO.
Other Devices by Cedic S.R.L.
Related Devices (Code: PIO)
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.