INTERFACE ARTERIAL BLOOD FILTER #40
K-Number: K823258 · 1982-11-24
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Device Summary
Frequently Asked Questions
What is the INTERFACE ARTERIAL BLOOD FILTER #40?
INTERFACE ARTERIAL BLOOD FILTER #40 is a medical device that received FDA 510(k) clearance on 1982-11-24. The listed applicant is Medical, Inc.. The 510(k) number is K823258.
When did INTERFACE ARTERIAL BLOOD FILTER #40 receive FDA 510(k) clearance?
INTERFACE ARTERIAL BLOOD FILTER #40 received FDA 510(k) clearance on 1982-11-24, under 510(k) number K823258.
Who is the listed applicant for INTERFACE ARTERIAL BLOOD FILTER #40?
The FDA 510(k) record lists Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTERFACE ARTERIAL BLOOD FILTER #40?
The FDA product code for INTERFACE ARTERIAL BLOOD FILTER #40 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 Medical, 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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