MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR
K-Number: K897068 · 1991-08-28
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Device Summary
Frequently Asked Questions
What is the MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR?
MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR is a medical device that received FDA 510(k) clearance on 1991-08-28. The listed applicant is Medtronic Vascular. The 510(k) number is K897068.
When did MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR receive FDA 510(k) clearance?
MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR received FDA 510(k) clearance on 1991-08-28, under 510(k) number K897068.
Who is the listed applicant for MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR?
The FDA product code for MEDTRONIC MINIMAX HOLLOW FIBER OXYGENATOR 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 Medtronic Vascular 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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