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FDA 510(k)

NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODE

K-Number: K130806 · 2013-07-12

ApplicantNeurovision Medical Products, Inc.
Decision Date2013-07-12
Product CodePDQ
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 2013-07-12 under 510(k) number K130806. The device is classified under product code PDQ. 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 2013-07-12. The listed applicant is Neurovision Medical Products, Inc.. The 510(k) number is K130806.

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 2013-07-12, under 510(k) number K130806.

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 PDQ.

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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 SENSORK113771SIGNAL GEAR URETHRAL CATHETER ELECTRODEK121931NONDISPOSABLE STIMULATING INSTRUMENTSK110989NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODEK110140NEUROVISION NERVE LOCATOR MONITORK110712DRYTOUCH SUCTION STIMULATOR PROBE

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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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