SYNAMPS2
K-Number: K023771 · 2003-02-06
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Device Summary
Frequently Asked Questions
What is the SYNAMPS2?
SYNAMPS2 is a medical device that received FDA 510(k) clearance on 2003-02-06. The listed applicant is Neuroscan. The 510(k) number is K023771.
When did SYNAMPS2 receive FDA 510(k) clearance?
SYNAMPS2 received FDA 510(k) clearance on 2003-02-06, under 510(k) number K023771.
Who is the listed applicant for SYNAMPS2?
The FDA 510(k) record lists Neuroscan as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNAMPS2?
The FDA product code for SYNAMPS2 is GWQ.
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 Neuroscan 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: GWQ)
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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