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FDA 510(k)

NUVANCE* FACIAL REJUVENATION SYSTEM

K-Number: K052953 · 2006-03-06

ApplicantETHICON, Inc.
Decision Date2006-03-06
Product CodeMXW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUVANCE* FACIAL REJUVENATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2006-03-06 under 510(k) number K052953. The device is classified under product code MXW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVANCE* FACIAL REJUVENATION SYSTEM?

NUVANCE* FACIAL REJUVENATION SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-06. The listed applicant is ETHICON, Inc.. The 510(k) number is K052953.

When did NUVANCE* FACIAL REJUVENATION SYSTEM receive FDA 510(k) clearance?

NUVANCE* FACIAL REJUVENATION SYSTEM received FDA 510(k) clearance on 2006-03-06, under 510(k) number K052953.

Who is the listed applicant for NUVANCE* FACIAL REJUVENATION SYSTEM?

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

What is the FDA product code for NUVANCE* FACIAL REJUVENATION SYSTEM?

The FDA product code for NUVANCE* FACIAL REJUVENATION SYSTEM is MXW.

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Related Devices (Code: MXW)

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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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