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FDA 510(k)

MAGNUM-20 (TM) INFLATION DEVICE

K-Number: K903621 · 1990-12-20

Decision Date1990-12-20
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAGNUM-20 (TM) INFLATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vascumed Systems. It received FDA 510(k) clearance on 1990-12-20 under 510(k) number K903621. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNUM-20 (TM) INFLATION DEVICE?

MAGNUM-20 (TM) INFLATION DEVICE is a medical device that received FDA 510(k) clearance on 1990-12-20. The listed applicant is Vascumed Systems. The 510(k) number is K903621.

When did MAGNUM-20 (TM) INFLATION DEVICE receive FDA 510(k) clearance?

MAGNUM-20 (TM) INFLATION DEVICE received FDA 510(k) clearance on 1990-12-20, under 510(k) number K903621.

Who is the listed applicant for MAGNUM-20 (TM) INFLATION DEVICE?

The FDA 510(k) record lists Vascumed Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNUM-20 (TM) INFLATION DEVICE?

The FDA product code for MAGNUM-20 (TM) INFLATION DEVICE is MAV.

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 Vascumed Systems 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: MAV)

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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