TRANSFUSION BLOOD FILTER
K-Number: K771862 · 1977-10-13
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Device Summary
Frequently Asked Questions
What is the TRANSFUSION BLOOD FILTER?
TRANSFUSION BLOOD FILTER is a medical device that received FDA 510(k) clearance on 1977-10-13. The listed applicant is Medical, Inc.. The 510(k) number is K771862.
When did TRANSFUSION BLOOD FILTER receive FDA 510(k) clearance?
TRANSFUSION BLOOD FILTER received FDA 510(k) clearance on 1977-10-13, under 510(k) number K771862.
Who is the listed applicant for TRANSFUSION BLOOD FILTER?
The FDA 510(k) record lists Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSFUSION BLOOD FILTER?
The FDA product code for TRANSFUSION BLOOD FILTER is FPB.
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 Medical, 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: FPB)
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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