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FDA 510(k)

ENTERAL FEEDING SPIKE ADAPTER

K-Number: K072652 · 2008-01-18

ApplicantCedic S.R.L.
Decision Date2008-01-18
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING SPIKE ADAPTER 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 2008-01-18 under 510(k) number K072652. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTERAL FEEDING SPIKE ADAPTER?

ENTERAL FEEDING SPIKE ADAPTER is a medical device that received FDA 510(k) clearance on 2008-01-18. The listed applicant is Cedic S.R.L.. The 510(k) number is K072652.

When did ENTERAL FEEDING SPIKE ADAPTER receive FDA 510(k) clearance?

ENTERAL FEEDING SPIKE ADAPTER received FDA 510(k) clearance on 2008-01-18, under 510(k) number K072652.

Who is the listed applicant for ENTERAL FEEDING SPIKE ADAPTER?

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 ENTERAL FEEDING SPIKE ADAPTER?

The FDA product code for ENTERAL FEEDING SPIKE ADAPTER is KNT.

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: KNT)

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.

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