SONOTRAX ULTRASONIC POCKET DOPPLER
K-Number: K040480 · 2004-05-25
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Device Summary
Frequently Asked Questions
What is the SONOTRAX ULTRASONIC POCKET DOPPLER?
SONOTRAX ULTRASONIC POCKET DOPPLER is a medical device that received FDA 510(k) clearance on 2004-05-25. The listed applicant is Edan Instruments, Inc.. The 510(k) number is K040480.
When did SONOTRAX ULTRASONIC POCKET DOPPLER receive FDA 510(k) clearance?
SONOTRAX ULTRASONIC POCKET DOPPLER received FDA 510(k) clearance on 2004-05-25, under 510(k) number K040480.
Who is the listed applicant for SONOTRAX ULTRASONIC POCKET DOPPLER?
The FDA 510(k) record lists Edan Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SONOTRAX ULTRASONIC POCKET DOPPLER?
The FDA product code for SONOTRAX ULTRASONIC POCKET DOPPLER is KNG.
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 Edan Instruments, 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: KNG)
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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