Cedic Enteral ENFit Transition Connectors
K-Number: K162254 · 2017-05-04
Device Summary
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. The listed applicant is Cedic S.R.L.. The 510(k) number is K162254.
When did Cedic Enteral ENFit Transition Connectors receive FDA 510(k) clearance?
Cedic Enteral ENFit Transition Connectors received FDA 510(k) clearance on 2017-05-04, under 510(k) number K162254.
Who is the listed applicant for Cedic Enteral ENFit Transition Connectors?
The FDA 510(k) record lists Cedic S.R.L. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Cedic S.R.L. as applicant
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.
Related Devices (Code: PIO)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.