NEUROMETRICS MONITOR
K-Number: K800452 · 1980-04-02
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Device Summary
Frequently Asked Questions
What is the NEUROMETRICS MONITOR?
NEUROMETRICS MONITOR is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Neurometrics. The 510(k) number is K800452.
When did NEUROMETRICS MONITOR receive FDA 510(k) clearance?
NEUROMETRICS MONITOR received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800452.
Who is the listed applicant for NEUROMETRICS MONITOR?
The FDA 510(k) record lists Neurometrics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROMETRICS MONITOR?
The FDA product code for NEUROMETRICS MONITOR is GWS.
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 Neurometrics 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: GWS)
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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