ENTERAL BAG/SET
K-Number: K880051 · 1988-04-14
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Device Summary
Frequently Asked Questions
What is the ENTERAL BAG/SET?
ENTERAL BAG/SET is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Churchill Corp.. The 510(k) number is K880051.
When did ENTERAL BAG/SET receive FDA 510(k) clearance?
ENTERAL BAG/SET received FDA 510(k) clearance on 1988-04-14, under 510(k) number K880051.
Who is the listed applicant for ENTERAL BAG/SET?
The FDA 510(k) record lists Churchill Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERAL BAG/SET?
The FDA product code for ENTERAL BAG/SET 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 Churchill Corp. 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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