ARTERIAL BLOOD FILTER BF-37
K-Number: K802755 · 1981-01-07
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Device Summary
Frequently Asked Questions
What is the ARTERIAL BLOOD FILTER BF-37?
ARTERIAL BLOOD FILTER BF-37 is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Delta Medical Industries. The 510(k) number is K802755.
When did ARTERIAL BLOOD FILTER BF-37 receive FDA 510(k) clearance?
ARTERIAL BLOOD FILTER BF-37 received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802755.
Who is the listed applicant for ARTERIAL BLOOD FILTER BF-37?
The FDA 510(k) record lists Delta Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIAL BLOOD FILTER BF-37?
The FDA product code for ARTERIAL BLOOD FILTER BF-37 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 Delta Medical Industries 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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