L.T.C. REPLACEMENT GASTROSTOMY TUBE
K-Number: K896621 · 1990-03-13
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Device Summary
Frequently Asked Questions
What is the L.T.C. REPLACEMENT GASTROSTOMY TUBE?
L.T.C. REPLACEMENT GASTROSTOMY TUBE is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Intl. Medical Marketing, Inc.. The 510(k) number is K896621.
When did L.T.C. REPLACEMENT GASTROSTOMY TUBE receive FDA 510(k) clearance?
L.T.C. REPLACEMENT GASTROSTOMY TUBE received FDA 510(k) clearance on 1990-03-13, under 510(k) number K896621.
Who is the listed applicant for L.T.C. REPLACEMENT GASTROSTOMY TUBE?
The FDA 510(k) record lists Intl. Medical Marketing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L.T.C. REPLACEMENT GASTROSTOMY TUBE?
The FDA product code for L.T.C. REPLACEMENT GASTROSTOMY TUBE is KCQ.
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 Intl. Medical Marketing, 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.
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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