ALBUMIN INTRAVENOUS ADMINISTRATION SET
K-Number: K791672 · 1979-10-26
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Device Summary
Frequently Asked Questions
What is the ALBUMIN INTRAVENOUS ADMINISTRATION SET?
ALBUMIN INTRAVENOUS ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Delmed, Inc.. The 510(k) number is K791672.
When did ALBUMIN INTRAVENOUS ADMINISTRATION SET receive FDA 510(k) clearance?
ALBUMIN INTRAVENOUS ADMINISTRATION SET received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791672.
Who is the listed applicant for ALBUMIN INTRAVENOUS ADMINISTRATION SET?
The FDA 510(k) record lists Delmed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALBUMIN INTRAVENOUS ADMINISTRATION SET?
The FDA product code for ALBUMIN INTRAVENOUS ADMINISTRATION SET is FPA.
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 Delmed, 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: FPA)
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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