LEVIN TUBE
K-Number: K830987 · 1983-05-27
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Device Summary
Frequently Asked Questions
What is the LEVIN TUBE?
LEVIN TUBE is a medical device that received FDA 510(k) clearance on 1983-05-27. The listed applicant is Medovations, Inc.. The 510(k) number is K830987.
When did LEVIN TUBE receive FDA 510(k) clearance?
LEVIN TUBE received FDA 510(k) clearance on 1983-05-27, under 510(k) number K830987.
Who is the listed applicant for LEVIN TUBE?
The FDA 510(k) record lists Medovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEVIN TUBE?
The FDA product code for LEVIN 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.
Other records listing Medovations, 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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