ARTERIAL BLOOD FILTER, MODEL AF-10
K-Number: K792450 · 1979-12-19
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Device Summary
Frequently Asked Questions
What is the ARTERIAL BLOOD FILTER, MODEL AF-10?
ARTERIAL BLOOD FILTER, MODEL AF-10 is a medical device that received FDA 510(k) clearance on 1979-12-19. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K792450.
When did ARTERIAL BLOOD FILTER, MODEL AF-10 receive FDA 510(k) clearance?
ARTERIAL BLOOD FILTER, MODEL AF-10 received FDA 510(k) clearance on 1979-12-19, under 510(k) number K792450.
Who is the listed applicant for ARTERIAL BLOOD FILTER, MODEL AF-10?
The FDA 510(k) record lists Bentley Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIAL BLOOD FILTER, MODEL AF-10?
The FDA product code for ARTERIAL BLOOD FILTER, MODEL AF-10 is DTM.
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 Bentley Laboratories, 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: DTM)
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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