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

DUAL SWITCH

K Number: K141908 · Decision Oct 22, 2014
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
18
Review Days
99

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Basic Information

Device Name
DUAL SWITCH
K Number
K141908
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Laser Engineering, Inc.
Date Received
July 15, 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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K Number Device Name
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K910062 02-10,001
K911852 COMPULSE CO2 SURGICAL LASER SYS.
K905676 MD CO2 SURGICAL LASER SYSTEM/GEN. SURGERY AND ORTH
K875314 GL-35 COLPOSCOPIC LASER SYSTEM
K881587 MODEL MD-25 CO2 LASER FOR PODIATRY APPLICATIONS
K881580 MODEL MD-25 CO2 LASER FOR DERMA./PLASTIC SURGERY
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