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FDA 510(k)

UVBIOTEK MODELS 3200B AND 4000B

K-Number: K051330 · 2005-11-18

ApplicantMedtek Lighting Corporation
Decision Date2005-11-18
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UVBIOTEK MODELS 3200B AND 4000B is the device name listed in this FDA 510(k) record. The listed applicant is Medtek Lighting Corporation. It received FDA 510(k) clearance on 2005-11-18 under 510(k) number K051330. 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 UVBIOTEK MODELS 3200B AND 4000B?

UVBIOTEK MODELS 3200B AND 4000B is a medical device that received FDA 510(k) clearance on 2005-11-18. The listed applicant is Medtek Lighting Corporation. The 510(k) number is K051330.

When did UVBIOTEK MODELS 3200B AND 4000B receive FDA 510(k) clearance?

UVBIOTEK MODELS 3200B AND 4000B received FDA 510(k) clearance on 2005-11-18, under 510(k) number K051330.

Who is the listed applicant for UVBIOTEK MODELS 3200B AND 4000B?

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

What is the FDA product code for UVBIOTEK MODELS 3200B AND 4000B?

The FDA product code for UVBIOTEK MODELS 3200B AND 4000B is FTC.

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Related Devices (Code: FTC)

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.

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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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