ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)
K-Number: K011077 · 2001-05-09
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Device Summary
Frequently Asked Questions
What is the ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)?
ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22) is a medical device that received FDA 510(k) clearance on 2001-05-09. The listed applicant is Andersen Products, Inc.. The 510(k) number is K011077.
When did ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22) receive FDA 510(k) clearance?
ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22) received FDA 510(k) clearance on 2001-05-09, under 510(k) number K011077.
Who is the listed applicant for ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)?
The FDA 510(k) record lists Andersen Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)?
The FDA product code for ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22) 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 Andersen Products, 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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