MODIFIED FEEDING JEJUNOSTOMY TUBE
K-Number: K800918 · 1980-07-28
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Device Summary
Frequently Asked Questions
What is the MODIFIED FEEDING JEJUNOSTOMY TUBE?
MODIFIED FEEDING JEJUNOSTOMY TUBE is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Mitchell V. Kaminski, Jr., M.D.. The 510(k) number is K800918.
When did MODIFIED FEEDING JEJUNOSTOMY TUBE receive FDA 510(k) clearance?
MODIFIED FEEDING JEJUNOSTOMY TUBE received FDA 510(k) clearance on 1980-07-28, under 510(k) number K800918.
Who is the listed applicant for MODIFIED FEEDING JEJUNOSTOMY TUBE?
The FDA 510(k) record lists Mitchell V. Kaminski, Jr., M.D. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED FEEDING JEJUNOSTOMY TUBE?
The FDA product code for MODIFIED FEEDING JEJUNOSTOMY 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.
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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