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

LIGHT SCALPEL

K Number: K141658 · Decision Oct 22, 2014
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
5
Review Days
124

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Basic Information

Device Name
LIGHT SCALPEL
K Number
K141658
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
Lightscalpel, LLC
Date Received
June 20, 2014
Decision Date
October 22, 2014
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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Other Clearances by Lightscalpel, LLC

K Number Device Name
K173827 LightScalpel
K132661 LIGHTSCALPEL
K123037 LIGHTSCALPEL
K121471 LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS