ULTIPOR SQ40S BLOOD TRANSFUSION FILTER
K-Number: K811985 · 1981-07-28
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Device Summary
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.
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
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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