INTERFACE ARTERIAL BLOOD FILTER
K-Number: K813131 · 1981-11-27
Advertisement
Device Summary
Frequently Asked Questions
What is the INTERFACE ARTERIAL BLOOD FILTER?
INTERFACE ARTERIAL BLOOD FILTER is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is Medical, Inc.. The 510(k) number is K813131.
When did INTERFACE ARTERIAL BLOOD FILTER receive FDA 510(k) clearance?
INTERFACE ARTERIAL BLOOD FILTER received FDA 510(k) clearance on 1981-11-27, under 510(k) number K813131.
Who is the listed applicant for INTERFACE ARTERIAL BLOOD FILTER?
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?
The FDA product code for INTERFACE ARTERIAL BLOOD FILTER 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.
Advertisement