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FDA 510(k)

MOBILE VERSA LIGHT

K-Number: K111049 · 2012-05-25

ApplicantMedtek Lighting Corp
Decision Date2012-05-25
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOBILE VERSA LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Medtek Lighting Corp. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K111049. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILE VERSA LIGHT?

MOBILE VERSA LIGHT is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Medtek Lighting Corp. The 510(k) number is K111049.

When did MOBILE VERSA LIGHT receive FDA 510(k) clearance?

MOBILE VERSA LIGHT received FDA 510(k) clearance on 2012-05-25, under 510(k) number K111049.

Who is the listed applicant for MOBILE VERSA LIGHT?

The FDA 510(k) record lists Medtek Lighting Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOBILE VERSA LIGHT?

The FDA product code for MOBILE VERSA LIGHT is FTC.

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Related Devices (Code: FTC)

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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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