ENTERAL ADMINISTRATION SET
K-Number: K870623 · 1987-06-26
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Device Summary
Frequently Asked Questions
What is the ENTERAL ADMINISTRATION SET?
ENTERAL ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1987-06-26. The listed applicant is Plasco, Inc.. The 510(k) number is K870623.
When did ENTERAL ADMINISTRATION SET receive FDA 510(k) clearance?
ENTERAL ADMINISTRATION SET received FDA 510(k) clearance on 1987-06-26, under 510(k) number K870623.
Who is the listed applicant for ENTERAL ADMINISTRATION SET?
The FDA 510(k) record lists Plasco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERAL ADMINISTRATION SET?
The FDA product code for ENTERAL ADMINISTRATION SET is FPD.
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 Plasco, 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: FPD)
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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