VIVONEX ACUTROL ENTERNAL FEEDING SYS
K-Number: K821067 · 1982-04-29
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Device Summary
Frequently Asked Questions
What is the VIVONEX ACUTROL ENTERNAL FEEDING SYS?
VIVONEX ACUTROL ENTERNAL FEEDING SYS is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Norwich Eaton Pharmaceuticals, Inc.. The 510(k) number is K821067.
When did VIVONEX ACUTROL ENTERNAL FEEDING SYS receive FDA 510(k) clearance?
VIVONEX ACUTROL ENTERNAL FEEDING SYS received FDA 510(k) clearance on 1982-04-29, under 510(k) number K821067.
Who is the listed applicant for VIVONEX ACUTROL ENTERNAL FEEDING SYS?
The FDA 510(k) record lists Norwich Eaton Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIVONEX ACUTROL ENTERNAL FEEDING SYS?
The FDA product code for VIVONEX ACUTROL ENTERNAL FEEDING SYS 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 Norwich Eaton Pharmaceuticals, 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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