BLOOD TRANSFUSION MICROFILTER
K-Number: K791809 · 1979-10-26
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Device Summary
Frequently Asked Questions
What is the BLOOD TRANSFUSION MICROFILTER?
BLOOD TRANSFUSION MICROFILTER is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Pioneer Viggo, Inc.. The 510(k) number is K791809.
When did BLOOD TRANSFUSION MICROFILTER receive FDA 510(k) clearance?
BLOOD TRANSFUSION MICROFILTER received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791809.
Who is the listed applicant for BLOOD TRANSFUSION MICROFILTER?
The FDA 510(k) record lists Pioneer Viggo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD TRANSFUSION MICROFILTER?
The FDA product code for BLOOD TRANSFUSION MICROFILTER 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 Pioneer Viggo, 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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