MAGNUM-20 (TM) INFLATION DEVICE
K-Number: K903621 · 1990-12-20
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Device Summary
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
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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