FILTER, TRANSFUSION BLOOD, INTERSEPT
K-Number: K760222 · 1976-08-06
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Device Summary
Frequently Asked Questions
What is the FILTER, TRANSFUSION BLOOD, INTERSEPT?
FILTER, TRANSFUSION BLOOD, INTERSEPT is a medical device that received FDA 510(k) clearance on 1976-08-06. The listed applicant is Surgikos, Inc.. The 510(k) number is K760222.
When did FILTER, TRANSFUSION BLOOD, INTERSEPT receive FDA 510(k) clearance?
FILTER, TRANSFUSION BLOOD, INTERSEPT received FDA 510(k) clearance on 1976-08-06, under 510(k) number K760222.
Who is the listed applicant for FILTER, TRANSFUSION BLOOD, INTERSEPT?
The FDA 510(k) record lists Surgikos, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FILTER, TRANSFUSION BLOOD, INTERSEPT?
The FDA product code for FILTER, TRANSFUSION BLOOD, INTERSEPT 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 Surgikos, 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: 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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