FASTRAC GASTRIC ACCESS PORT KIT
K-Number: K033562 · 2003-12-12
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Device Summary
Frequently Asked Questions
What is the FASTRAC GASTRIC ACCESS PORT KIT?
FASTRAC GASTRIC ACCESS PORT KIT is a medical device that received FDA 510(k) clearance on 2003-12-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K033562.
When did FASTRAC GASTRIC ACCESS PORT KIT receive FDA 510(k) clearance?
FASTRAC GASTRIC ACCESS PORT KIT received FDA 510(k) clearance on 2003-12-12, under 510(k) number K033562.
Who is the listed applicant for FASTRAC GASTRIC ACCESS PORT KIT?
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 FASTRAC GASTRIC ACCESS PORT KIT?
The FDA product code for FASTRAC GASTRIC ACCESS PORT KIT 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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