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FDA 510(k)

CARTMILL/BARRY FEEDING TUBE

K-Number: K812427 · 1981-09-23

ApplicantImpra, Inc.
Decision Date1981-09-23
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CARTMILL/BARRY FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Impra, Inc.. It received FDA 510(k) clearance on 1981-09-23 under 510(k) number K812427. 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 CARTMILL/BARRY FEEDING TUBE?

CARTMILL/BARRY FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1981-09-23. The listed applicant is Impra, Inc.. The 510(k) number is K812427.

When did CARTMILL/BARRY FEEDING TUBE receive FDA 510(k) clearance?

CARTMILL/BARRY FEEDING TUBE received FDA 510(k) clearance on 1981-09-23, under 510(k) number K812427.

Who is the listed applicant for CARTMILL/BARRY FEEDING TUBE?

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

What is the FDA product code for CARTMILL/BARRY FEEDING TUBE?

The FDA product code for CARTMILL/BARRY FEEDING TUBE 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 Impra, 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 29 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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