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FDA 510(k)

MAXIMA PLUS HOLLOW FIBER OXYGENATOR

K-Number: K941473 · 1995-06-21

Decision Date1995-06-21
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAXIMA PLUS HOLLOW FIBER OXYGENATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-06-21 under 510(k) number K941473. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXIMA PLUS HOLLOW FIBER OXYGENATOR?

MAXIMA PLUS HOLLOW FIBER OXYGENATOR is a medical device that received FDA 510(k) clearance on 1995-06-21. The listed applicant is Medtronic Vascular. The 510(k) number is K941473.

When did MAXIMA PLUS HOLLOW FIBER OXYGENATOR receive FDA 510(k) clearance?

MAXIMA PLUS HOLLOW FIBER OXYGENATOR received FDA 510(k) clearance on 1995-06-21, under 510(k) number K941473.

Who is the listed applicant for MAXIMA PLUS 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 MAXIMA PLUS HOLLOW FIBER OXYGENATOR?

The FDA product code for MAXIMA PLUS 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.

View all 474 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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