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FDA 510(k)

40 MICRON BLOOD TRANSFUSION FILTER

K-Number: K941628 · 1995-02-16

Decision Date1995-02-16
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

40 MICRON BLOOD TRANSFUSION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products Corp.. It received FDA 510(k) clearance on 1995-02-16 under 510(k) number K941628. 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 40 MICRON BLOOD TRANSFUSION FILTER?

40 MICRON BLOOD TRANSFUSION FILTER is a medical device that received FDA 510(k) clearance on 1995-02-16. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K941628.

When did 40 MICRON BLOOD TRANSFUSION FILTER receive FDA 510(k) clearance?

40 MICRON BLOOD TRANSFUSION FILTER received FDA 510(k) clearance on 1995-02-16, under 510(k) number K941628.

Who is the listed applicant for 40 MICRON BLOOD TRANSFUSION FILTER?

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 40 MICRON BLOOD TRANSFUSION FILTER?

The FDA product code for 40 MICRON BLOOD TRANSFUSION 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 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.

View all 19 devices →

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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