SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM
K-Number: K022858 · 2002-09-06
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Device Summary
Frequently Asked Questions
What is the SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM?
SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is Novasonics, Inc.. The 510(k) number is K022858.
When did SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM receive FDA 510(k) clearance?
SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM received FDA 510(k) clearance on 2002-09-06, under 510(k) number K022858.
Who is the listed applicant for SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM?
The FDA 510(k) record lists Novasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM?
The FDA product code for SUPERNOVA DIAGNOSTIC ULTRASOUND SCANNING SYSTEM is IYN.
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.
Related Devices (Code: IYN)
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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