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

Picasso Pro Diode Laser (002-00460)

K Number: K254197 · Decision Mar 11, 2026
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
31
Review Days
78

Basic Information

Device Name
Picasso Pro Diode Laser (002-00460)
K Number
K254197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAO Group, Inc.
Date Received
December 23, 2025
Decision Date
March 11, 2026
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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