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FDA 510(k)

Perceptive electric dental motor and control unit

K-Number: K220873 · 2022-12-15

ApplicantLares Research
Decision Date2022-12-15
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Perceptive electric dental motor and control unit is a medical device manufactured by Lares Research. It received FDA 510(k) clearance on 2022-12-15 under approval number K220873. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Perceptive electric dental motor and control unit?

Perceptive electric dental motor and control unit is a medical device that received FDA 510(k) clearance on 2022-12-15. It is manufactured by Lares Research. The 510(k) number is K220873.

When was Perceptive electric dental motor and control unit approved by the FDA?

Perceptive electric dental motor and control unit received FDA 510(k) clearance on 2022-12-15, under approval number K220873.

What company makes Perceptive electric dental motor and control unit?

Perceptive electric dental motor and control unit is manufactured by Lares Research.

What is the FDA product code for Perceptive electric dental motor and control unit?

The FDA product code for Perceptive electric dental motor and control unit is EIA.

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Other Devices by Lares Research

K220874Smooth Drive contra angle and straight handpieces

Related Devices (Code: EIA)

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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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