ENTERAL DELIVERY SET
K-Number: K831168 · 1983-05-09
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Device Summary
Frequently Asked Questions
What is the ENTERAL DELIVERY SET?
ENTERAL DELIVERY SET is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K831168.
When did ENTERAL DELIVERY SET receive FDA 510(k) clearance?
ENTERAL DELIVERY SET received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831168.
Who is the listed applicant for ENTERAL DELIVERY SET?
The FDA 510(k) record lists Biosearch Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERAL DELIVERY SET?
The FDA product code for ENTERAL DELIVERY 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 Biosearch Medical 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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