BARD(R) JEJUNAL FEEDING/GASTRIC DECOMPRESSION TUBES
K-Number: K946249 · 1995-12-11
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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