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FDA 510(k)

ULTIPOR SQ40S BLOOD TRANSFUSION FILTER

K-Number: K811985 · 1981-07-28

Decision Date1981-07-28
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTIPOR SQ40S BLOOD TRANSFUSION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Pall Biomedical Products Co.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811985. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIPOR SQ40S BLOOD TRANSFUSION FILTER?

ULTIPOR SQ40S BLOOD TRANSFUSION FILTER is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K811985.

When did ULTIPOR SQ40S BLOOD TRANSFUSION FILTER receive FDA 510(k) clearance?

ULTIPOR SQ40S BLOOD TRANSFUSION FILTER received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811985.

Who is the listed applicant for ULTIPOR SQ40S BLOOD TRANSFUSION FILTER?

The FDA 510(k) record lists Pall Biomedical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTIPOR SQ40S BLOOD TRANSFUSION FILTER?

The FDA product code for ULTIPOR SQ40S BLOOD TRANSFUSION FILTER is CAK.

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 Pall Biomedical Products Co. 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 28 devices →

Related Devices (Code: CAK)

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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