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FDA 510(k)

LIVE VIEW PANEL (LVP)

K-Number: K131415 · 2013-08-09

ApplicantNeurotronics, Inc.
Decision Date2013-08-09
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LIVE VIEW PANEL (LVP) is the device name listed in this FDA 510(k) record. The listed applicant is Neurotronics, Inc.. It received FDA 510(k) clearance on 2013-08-09 under 510(k) number K131415. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIVE VIEW PANEL (LVP)?

LIVE VIEW PANEL (LVP) is a medical device that received FDA 510(k) clearance on 2013-08-09. The listed applicant is Neurotronics, Inc.. The 510(k) number is K131415.

When did LIVE VIEW PANEL (LVP) receive FDA 510(k) clearance?

LIVE VIEW PANEL (LVP) received FDA 510(k) clearance on 2013-08-09, under 510(k) number K131415.

Who is the listed applicant for LIVE VIEW PANEL (LVP)?

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

What is the FDA product code for LIVE VIEW PANEL (LVP)?

The FDA product code for LIVE VIEW PANEL (LVP) is OLV.

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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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