MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER
K-Number: K881263 · 1990-01-05
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Device Summary
Frequently Asked Questions
What is the MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER?
MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER is a medical device that received FDA 510(k) clearance on 1990-01-05. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K881263.
When did MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER receive FDA 510(k) clearance?
MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER received FDA 510(k) clearance on 1990-01-05, under 510(k) number K881263.
Who is the listed applicant for MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER?
The FDA 510(k) record lists Multigon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER?
The FDA product code for MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER is HGL.
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 Multigon Industries, Inc. 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: HGL)
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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