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FDA 510(k)

CLINIFEEDING SYSTEM 1

K-Number: K791758 · 1979-10-26

ApplicantRoussel (Canada) , Ltd.
Decision Date1979-10-26
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLINIFEEDING SYSTEM 1 is the device name listed in this FDA 510(k) record. The listed applicant is Roussel (Canada) , Ltd.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791758. 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 CLINIFEEDING SYSTEM 1?

CLINIFEEDING SYSTEM 1 is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Roussel (Canada) , Ltd.. The 510(k) number is K791758.

When did CLINIFEEDING SYSTEM 1 receive FDA 510(k) clearance?

CLINIFEEDING SYSTEM 1 received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791758.

Who is the listed applicant for CLINIFEEDING SYSTEM 1?

The FDA 510(k) record lists Roussel (Canada) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINIFEEDING SYSTEM 1?

The FDA product code for CLINIFEEDING SYSTEM 1 is KNT.

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Related Devices (Code: KNT)

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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.

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