BLOOD OXYGENATOR 5070
K-Number: K831894 · 1983-10-20
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Device Summary
Frequently Asked Questions
What is the BLOOD OXYGENATOR 5070?
BLOOD OXYGENATOR 5070 is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Shiley, Inc.. The 510(k) number is K831894.
When did BLOOD OXYGENATOR 5070 receive FDA 510(k) clearance?
BLOOD OXYGENATOR 5070 received FDA 510(k) clearance on 1983-10-20, under 510(k) number K831894.
Who is the listed applicant for BLOOD OXYGENATOR 5070?
The FDA 510(k) record lists Shiley, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD OXYGENATOR 5070?
The FDA product code for BLOOD OXYGENATOR 5070 is DTZ.
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 Shiley, 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: DTZ)
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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