AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT
K-Number: K123716 · 2013-04-19
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Device Summary
Frequently Asked Questions
What is the AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT?
AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT is a medical device that received FDA 510(k) clearance on 2013-04-19. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K123716.
When did AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT receive FDA 510(k) clearance?
AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT received FDA 510(k) clearance on 2013-04-19, under 510(k) number K123716.
Who is the listed applicant for AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT?
The FDA 510(k) record lists Applied Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE KIT?
The FDA product code for AMT LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE 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 Applied Medical Technology, 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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