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FDA 510(k)

ESTHETICA

K-Number: K100083 · 2010-03-19

ApplicantKerr Corporation
Decision Date2010-03-19
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ESTHETICA is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2010-03-19 under 510(k) number K100083. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESTHETICA?

ESTHETICA is a medical device that received FDA 510(k) clearance on 2010-03-19. The listed applicant is Kerr Corporation. The 510(k) number is K100083.

When did ESTHETICA receive FDA 510(k) clearance?

ESTHETICA received FDA 510(k) clearance on 2010-03-19, under 510(k) number K100083.

Who is the listed applicant for ESTHETICA?

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

What is the FDA product code for ESTHETICA?

The FDA product code for ESTHETICA is EBF.

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Related Devices (Code: EBF)

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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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