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FDA 510(k)

Complement Kit Cases

K-Number: K230804 · 2023-07-07

Decision Date2023-07-07
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Complement Kit Cases is a medical device manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. It received FDA 510(k) clearance on 2023-07-07 under approval number K230804. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Complement Kit Cases?

Complement Kit Cases is a medical device that received FDA 510(k) clearance on 2023-07-07. It is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K230804.

When was Complement Kit Cases approved by the FDA?

Complement Kit Cases received FDA 510(k) clearance on 2023-07-07, under approval number K230804.

What company makes Complement Kit Cases?

Complement Kit Cases is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A..

What is the FDA product code for Complement Kit Cases?

The FDA product code for Complement Kit Cases is KCT.

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Official Source

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