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FDA 510(k)

ALBUMIN INTRAVENOUS ADMINISTRATION SET

K-Number: K791672 · 1979-10-26

ApplicantDelmed, Inc.
Decision Date1979-10-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALBUMIN INTRAVENOUS ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Delmed, Inc.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791672. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 27 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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