NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8
K-Number: K001692 · 2000-11-24
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Device Summary
Frequently Asked Questions
What is the NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8?
NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8 is a medical device that received FDA 510(k) clearance on 2000-11-24. The listed applicant is Neurosoft, Inc.. The 510(k) number is K001692.
When did NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8 receive FDA 510(k) clearance?
NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8 received FDA 510(k) clearance on 2000-11-24, under 510(k) number K001692.
Who is the listed applicant for NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8?
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 NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8?
The FDA product code for NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8 is JXE.
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: JXE)
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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