STOMACH TUBES
K-Number: K800508 · 1980-04-08
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Device Summary
Frequently Asked Questions
What is the STOMACH TUBES?
STOMACH TUBES is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is Medi-Craft , Ltd.. The 510(k) number is K800508.
When did STOMACH TUBES receive FDA 510(k) clearance?
STOMACH TUBES received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800508.
Who is the listed applicant for STOMACH TUBES?
The FDA 510(k) record lists Medi-Craft , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOMACH TUBES?
The FDA product code for STOMACH 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 Medi-Craft , Ltd. 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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