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FDA 510(k)

ALMA LASERS FAMILY OF PIXEL RF TIPS

K-Number: K121150 · 2012-09-21

ApplicantAlma Lasers, Inc.
Decision Date2012-09-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALMA LASERS FAMILY OF PIXEL RF TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Alma Lasers, Inc.. It received FDA 510(k) clearance on 2012-09-21 under 510(k) number K121150. 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 ALMA LASERS FAMILY OF PIXEL RF TIPS?

ALMA LASERS FAMILY OF PIXEL RF TIPS is a medical device that received FDA 510(k) clearance on 2012-09-21. The listed applicant is Alma Lasers, Inc.. The 510(k) number is K121150.

When did ALMA LASERS FAMILY OF PIXEL RF TIPS receive FDA 510(k) clearance?

ALMA LASERS FAMILY OF PIXEL RF TIPS received FDA 510(k) clearance on 2012-09-21, under 510(k) number K121150.

Who is the listed applicant for ALMA LASERS FAMILY OF PIXEL RF TIPS?

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

What is the FDA product code for ALMA LASERS FAMILY OF PIXEL RF TIPS?

The FDA product code for ALMA LASERS FAMILY OF PIXEL RF TIPS 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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