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FDA 510(k)

GRT LITE, MODEL 8-A

K-Number: K050668 · 2006-02-03

ApplicantGrt Solutions, Inc.
Decision Date2006-02-03
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRT LITE, MODEL 8-A is the device name listed in this FDA 510(k) record. The listed applicant is Grt Solutions, Inc.. It received FDA 510(k) clearance on 2006-02-03 under 510(k) number K050668. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRT LITE, MODEL 8-A?

GRT LITE, MODEL 8-A is a medical device that received FDA 510(k) clearance on 2006-02-03. The listed applicant is Grt Solutions, Inc.. The 510(k) number is K050668.

When did GRT LITE, MODEL 8-A receive FDA 510(k) clearance?

GRT LITE, MODEL 8-A received FDA 510(k) clearance on 2006-02-03, under 510(k) number K050668.

Who is the listed applicant for GRT LITE, MODEL 8-A?

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

What is the FDA product code for GRT LITE, MODEL 8-A?

The FDA product code for GRT LITE, MODEL 8-A is NHN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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