NEUROSOFT'S SOURCE
K-Number: K011241 · 2001-09-19
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Device Summary
Frequently Asked Questions
What is the NEUROSOFT'S SOURCE?
NEUROSOFT'S SOURCE is a medical device that received FDA 510(k) clearance on 2001-09-19. The listed applicant is Neurosoft, Inc.. The 510(k) number is K011241.
When did NEUROSOFT'S SOURCE receive FDA 510(k) clearance?
NEUROSOFT'S SOURCE received FDA 510(k) clearance on 2001-09-19, under 510(k) number K011241.
Who is the listed applicant for NEUROSOFT'S SOURCE?
The FDA 510(k) record lists Neurosoft, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROSOFT'S SOURCE?
The FDA product code for NEUROSOFT'S SOURCE is OLX.
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 Neurosoft, 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: OLX)
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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