Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KANGAROO ENTERAL FEEDING PUMP

K-Number: K801725 · 1980-08-13

Decision Date1980-08-13
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KANGAROO ENTERAL FEEDING PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801725. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KANGAROO ENTERAL FEEDING PUMP?

KANGAROO ENTERAL FEEDING PUMP is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K801725.

When did KANGAROO ENTERAL FEEDING PUMP receive FDA 510(k) clearance?

KANGAROO ENTERAL FEEDING PUMP received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801725.

Who is the listed applicant for KANGAROO ENTERAL FEEDING PUMP?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KANGAROO ENTERAL FEEDING PUMP?

The FDA product code for KANGAROO ENTERAL FEEDING PUMP is FRN.

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 Chesebrough-Pond'S U.S.A. Co. 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.

View all 33 devices →

Related Devices (Code: FRN)

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.

↑