RECTAL TUBES
K-Number: K830986 · 1983-05-27
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Device Summary
Frequently Asked Questions
What is the RECTAL TUBES?
RECTAL TUBES 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 K830986.
When did RECTAL TUBES receive FDA 510(k) clearance?
RECTAL TUBES received FDA 510(k) clearance on 1983-05-27, under 510(k) number K830986.
Who is the listed applicant for RECTAL TUBES?
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 RECTAL TUBES?
The FDA product code for RECTAL 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 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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