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FDA 510(k)

BLOOD TRANSFUSION MICROFILTER

K-Number: K791809 · 1979-10-26

Decision Date1979-10-26
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLOOD TRANSFUSION MICROFILTER is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Viggo, Inc.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791809. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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