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FDA 510(k)

NEURO WAVE 6

K-Number: K062003 · 2007-09-19

ApplicantLhasa Oms, Inc.
Decision Date2007-09-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURO WAVE 6 is the device name listed in this FDA 510(k) record. The listed applicant is Lhasa Oms, Inc.. It received FDA 510(k) clearance on 2007-09-19 under 510(k) number K062003. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURO WAVE 6?

NEURO WAVE 6 is a medical device that received FDA 510(k) clearance on 2007-09-19. The listed applicant is Lhasa Oms, Inc.. The 510(k) number is K062003.

When did NEURO WAVE 6 receive FDA 510(k) clearance?

NEURO WAVE 6 received FDA 510(k) clearance on 2007-09-19, under 510(k) number K062003.

Who is the listed applicant for NEURO WAVE 6?

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

What is the FDA product code for NEURO WAVE 6?

The FDA product code for NEURO WAVE 6 is GZJ.

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Related Devices (Code: GZJ)

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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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