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FDA 510(k)

MVR COLLAPSIBLE VENOUS RESERVOIR BAG

K-Number: K920774 · 1992-10-19

Decision Date1992-10-19
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MVR COLLAPSIBLE VENOUS RESERVOIR BAG is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1992-10-19 under 510(k) number K920774. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVR COLLAPSIBLE VENOUS RESERVOIR BAG?

MVR COLLAPSIBLE VENOUS RESERVOIR BAG is a medical device that received FDA 510(k) clearance on 1992-10-19. The listed applicant is Medtronic Vascular. The 510(k) number is K920774.

When did MVR COLLAPSIBLE VENOUS RESERVOIR BAG receive FDA 510(k) clearance?

MVR COLLAPSIBLE VENOUS RESERVOIR BAG received FDA 510(k) clearance on 1992-10-19, under 510(k) number K920774.

Who is the listed applicant for MVR COLLAPSIBLE VENOUS RESERVOIR BAG?

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 MVR COLLAPSIBLE VENOUS RESERVOIR BAG?

The FDA product code for MVR COLLAPSIBLE VENOUS RESERVOIR BAG is DTN.

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: DTN)

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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