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FDA 510(k)

Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes

K-Number: K181787 · 2019-04-25

ApplicantCedic S.R.L.
Decision Date2019-04-25
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes is the device name listed in this FDA 510(k) record. The listed applicant is Cedic S.R.L.. It received FDA 510(k) clearance on 2019-04-25 under 510(k) number K181787. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes?

Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes is a medical device that received FDA 510(k) clearance on 2019-04-25. The listed applicant is Cedic S.R.L.. The 510(k) number is K181787.

When did Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes receive FDA 510(k) clearance?

Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes received FDA 510(k) clearance on 2019-04-25, under 510(k) number K181787.

Who is the listed applicant for Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes?

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 Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes?

The FDA product code for Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes is PIF.

Related Clinical Trials

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.

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: PIF)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.