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FDA 510(k)

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)

K-Number: K092195 · 2009-10-01

ApplicantCutera, Inc.
Decision Date2009-10-01
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is the device name listed in this FDA 510(k) record. The listed applicant is Cutera, Inc.. It received FDA 510(k) clearance on 2009-10-01 under 510(k) number K092195. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is a medical device that received FDA 510(k) clearance on 2009-10-01. The listed applicant is Cutera, Inc.. The 510(k) number is K092195.

When did CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) receive FDA 510(k) clearance?

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) received FDA 510(k) clearance on 2009-10-01, under 510(k) number K092195.

Who is the listed applicant for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

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

What is the FDA product code for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)?

The FDA product code for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD) is NUV.

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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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