FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

The Alma Opus System, Colibri Applicator and Tips

K Number: K201520 · Decision Oct 27, 2021
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
20
Review Days
506

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Basic Information

Device Name
The Alma Opus System, Colibri Applicator and Tips
K Number
K201520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alma Lasers, Inc.
Date Received
June 8, 2020
Decision Date
October 27, 2021
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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