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FDA 510(k)

BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES

K-Number: K946249 · 1995-12-11

Decision Date1995-12-11
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K946249. 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 BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES?

BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K946249.

When did BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES receive FDA 510(k) clearance?

BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES received FDA 510(k) clearance on 1995-12-11, under 510(k) number K946249.

Who is the listed applicant for BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES?

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

What is the FDA product code for BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES?

The FDA product code for BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES 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 C.R. Bard, 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 616 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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