BLOOD ADMINISTRATION SET
K-Number: K920788 · 1992-06-04
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Device Summary
Frequently Asked Questions
What is the BLOOD ADMINISTRATION SET?
BLOOD ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K920788.
When did BLOOD ADMINISTRATION SET receive FDA 510(k) clearance?
BLOOD ADMINISTRATION SET received FDA 510(k) clearance on 1992-06-04, under 510(k) number K920788.
Who is the listed applicant for BLOOD ADMINISTRATION SET?
The FDA 510(k) record lists Douglas Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD ADMINISTRATION SET?
The FDA product code for BLOOD ADMINISTRATION SET is BRZ.
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 Douglas Medical Products Corp. 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: BRZ)
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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