EXPLORER CVS TRANSCRANIAL DOPPLER
K-Number: K990517 · 2000-08-01
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Device Summary
Frequently Asked Questions
What is the EXPLORER CVS TRANSCRANIAL DOPPLER?
EXPLORER CVS TRANSCRANIAL DOPPLER is a medical device that received FDA 510(k) clearance on 2000-08-01. The listed applicant is Diagnostic Medical Systems. The 510(k) number is K990517.
When did EXPLORER CVS TRANSCRANIAL DOPPLER receive FDA 510(k) clearance?
EXPLORER CVS TRANSCRANIAL DOPPLER received FDA 510(k) clearance on 2000-08-01, under 510(k) number K990517.
Who is the listed applicant for EXPLORER CVS TRANSCRANIAL DOPPLER?
The FDA 510(k) record lists Diagnostic Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXPLORER CVS TRANSCRANIAL DOPPLER?
The FDA product code for EXPLORER CVS TRANSCRANIAL DOPPLER 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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