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FDA 510(k)

FILTER, TRANSFUSION BLOOD, INTERSEPT

K-Number: K760222 · 1976-08-06

Decision Date1976-08-06
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTER, TRANSFUSION BLOOD, INTERSEPT is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1976-08-06 under 510(k) number K760222. 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 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.

View all 56 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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