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FDA 510(k)

NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE

K-Number: K110989 · 2011-11-03

ApplicantNeurovision Medical Products, Inc.
Decision Date2011-11-03
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE 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 2011-11-03 under 510(k) number K110989. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE?

NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE is a medical device that received FDA 510(k) clearance on 2011-11-03. The listed applicant is Neurovision Medical Products, Inc.. The 510(k) number is K110989.

When did NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE receive FDA 510(k) clearance?

NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE received FDA 510(k) clearance on 2011-11-03, under 510(k) number K110989.

Who is the listed applicant for NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE?

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 INK PRINTED ENDOTRACHEAL TUBE ELECTRODE?

The FDA product code for NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE is ETN.

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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 INSTRUMENTSK110140NEUROVISION NERVE LOCATOR MONITORK110712DRYTOUCH SUCTION STIMULATOR PROBE

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Related Devices (Code: ETN)

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.

K253536Evala Nerve Stimulator (EPNR002)Epineuron Technologies, Inc.K251672NIM Essence™ EMG Endotracheal Tube (NIMEID060); NIM Essence™ EMG Endotracheal Tube (NIMEID065); NIM Essence™ EMG Endotracheal Tube (NIMEID070); NIM Essence™ EMG Endotracheal Tube (NIMEID075); NIM Essence™ EMG Endotracheal Tube (NIMEID080)Medtronic Xomed, Inc.K242852ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM Tube I.D. 8.0, O.D. 11.0 (520847)Inomed Medizintechnik GmbHK233001Bioscope Neuromonitor DeviceBiosys Biyomedikal Muhendislik San. VE Tic. A.S.K241917EARP Nerve Cuff ElectrodeRetropsoas Technologies, LLCK232888Disposable Laryngeal ElectrodesSuzhou Haishen Medical Device Associates Co., Ltd.

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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