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FDA 510(k)

MATRIX RF APPLICATOR

K-Number: K090025 · 2010-01-08

ApplicantSyneron Medical, Ltd.
Decision Date2010-01-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MATRIX RF APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Syneron Medical, Ltd.. It received FDA 510(k) clearance on 2010-01-08 under 510(k) number K090025. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX RF APPLICATOR?

MATRIX RF APPLICATOR is a medical device that received FDA 510(k) clearance on 2010-01-08. The listed applicant is Syneron Medical, Ltd.. The 510(k) number is K090025.

When did MATRIX RF APPLICATOR receive FDA 510(k) clearance?

MATRIX RF APPLICATOR received FDA 510(k) clearance on 2010-01-08, under 510(k) number K090025.

Who is the listed applicant for MATRIX RF APPLICATOR?

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

What is the FDA product code for MATRIX RF APPLICATOR?

The FDA product code for MATRIX RF APPLICATOR is GEI.

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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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