CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY
K-Number: K920156 · 1992-03-16
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Device Summary
Frequently Asked Questions
What is the CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY?
CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY is a medical device that received FDA 510(k) clearance on 1992-03-16. The listed applicant is Clinical Neuro Systems, LLC. The 510(k) number is K920156.
When did CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY receive FDA 510(k) clearance?
CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY received FDA 510(k) clearance on 1992-03-16, under 510(k) number K920156.
Who is the listed applicant for CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY?
The FDA 510(k) record lists Clinical Neuro Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY?
The FDA product code for CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY is JXG.
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 Clinical Neuro Systems, LLC 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: JXG)
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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