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FDA 510(k)

Neodent Instrument Kit Cases

K-Number: K190665 · 2019-12-23

ApplicantJjgc Industria E Comercio DE Materiais Dentarios S.A.
Decision Date2019-12-23
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Neodent Instrument Kit Cases is a medical device manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2019-12-23 under approval number K190665. 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 Neodent Instrument Kit Cases?

Neodent Instrument Kit Cases is a medical device that received FDA 510(k) clearance on 2019-12-23. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K190665.

When was Neodent Instrument Kit Cases approved by the FDA?

Neodent Instrument Kit Cases received FDA 510(k) clearance on 2019-12-23, under approval number K190665.

What company makes Neodent Instrument Kit Cases?

Neodent Instrument Kit Cases is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..

What is the FDA product code for Neodent Instrument Kit Cases?

The FDA product code for Neodent Instrument Kit Cases is KCT.

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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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