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FDA 510(k)

NEUROVISION NERVE LOCATOR MONITOR

K-Number: K110140 · 2011-09-30

ApplicantNeurovision Medical Products, Inc.
Decision Date2011-09-30
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROVISION NERVE LOCATOR MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Neurovision Medical Products, Inc.. It received FDA 510(k) clearance on 2011-09-30 under 510(k) number K110140. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROVISION NERVE LOCATOR MONITOR?

NEUROVISION NERVE LOCATOR MONITOR is a medical device that received FDA 510(k) clearance on 2011-09-30. The listed applicant is Neurovision Medical Products, Inc.. The 510(k) number is K110140.

When did NEUROVISION NERVE LOCATOR MONITOR receive FDA 510(k) clearance?

NEUROVISION NERVE LOCATOR MONITOR received FDA 510(k) clearance on 2011-09-30, under 510(k) number K110140.

Who is the listed applicant for NEUROVISION NERVE LOCATOR MONITOR?

The FDA 510(k) record lists Neurovision Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROVISION NERVE LOCATOR MONITOR?

The FDA product code for NEUROVISION NERVE LOCATOR MONITOR is GWF.

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Other records listing Neurovision Medical Products, 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.

K130570NEUROVISION MEDICAL MOTION SENSORK130806NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODEK113771SIGNAL GEAR URETHRAL CATHETER ELECTRODEK121931NONDISPOSABLE STIMULATING INSTRUMENTSK110989NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODEK110712DRYTOUCH SUCTION STIMULATOR PROBE

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Related Devices (Code: GWF)

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.

K263010ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpressinomed Medizintechnik GmbHK253301BraiN20® (BraiN20)Time IS Brain, S.L.K252842SafeOp 3: Neural Informatix SystemAlphatec Spine, Inc.K243982Nicolet EDXNatus Neurology IncorporatedK243495Natus Ultrapro S100 (982A0594)Natus Neurology IncorporatedK242345Delphi StimulatorQuantalx Neuroscience

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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