QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM
K-Number: K860581 · 1987-02-13
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Device Summary
Frequently Asked Questions
What is the QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM?
QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Quantum Medical Systems, Inc.. The 510(k) number is K860581.
When did QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM receive FDA 510(k) clearance?
QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM received FDA 510(k) clearance on 1987-02-13, under 510(k) number K860581.
Who is the listed applicant for QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM?
The FDA 510(k) record lists Quantum Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM?
The FDA product code for QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM is IYO.
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 Quantum Medical Systems, 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: IYO)
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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