PEDIATRIC ARTERIAL BLOOD FILTER #AF-540
K-Number: K820679 · 1982-06-17
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Device Summary
Frequently Asked Questions
What is the PEDIATRIC ARTERIAL BLOOD FILTER #AF-540?
PEDIATRIC ARTERIAL BLOOD FILTER #AF-540 is a medical device that received FDA 510(k) clearance on 1982-06-17. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K820679.
When did PEDIATRIC ARTERIAL BLOOD FILTER #AF-540 receive FDA 510(k) clearance?
PEDIATRIC ARTERIAL BLOOD FILTER #AF-540 received FDA 510(k) clearance on 1982-06-17, under 510(k) number K820679.
Who is the listed applicant for PEDIATRIC ARTERIAL BLOOD FILTER #AF-540?
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 PEDIATRIC ARTERIAL BLOOD FILTER #AF-540?
The FDA product code for PEDIATRIC ARTERIAL BLOOD FILTER #AF-540 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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