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FDA 510(k)

KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS

K-Number: K973409 · 1998-02-27

Decision Date1998-02-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1998-02-27 under 510(k) number K973409. 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 KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS?

KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS is a medical device that received FDA 510(k) clearance on 1998-02-27. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K973409.

When did KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS receive FDA 510(k) clearance?

KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS received FDA 510(k) clearance on 1998-02-27, under 510(k) number K973409.

Who is the listed applicant for KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS?

The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS?

The FDA product code for KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS 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 Davis & Geck, Inc. 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 45 devices →

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

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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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