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

VICTUS FEMTOSECOND LASER PLATFORM

K Number: K122386 · Decision Feb 8, 2013
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
46
Applicant Total
10
Review Days
186

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Basic Information

Device Name
VICTUS FEMTOSECOND LASER PLATFORM
K Number
K122386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Technolas Perfect Vision GmbH
Date Received
August 6, 2012
Decision Date
February 8, 2013
Product Code
OOE
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
OOE Ophthalmic Femtosecond Laser

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K Number Device Name
K200724 VICTUS Femtosecond Laser Platform
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K151161 VICTUS Femtosecond Laser Platform
K141379 VICTUS FEMTOSECOND LASER PLATFORM
K140615 VICTUS FEMTOSECOND LASER PLATFORM
K132534 VICTUS FEMTOSECOND LASER PLATFORM
K120426 VICTUS LASER PLATFORM
K110427 FEMTEC LASER SYSTEM FOR CAPSULOTOMY
K984443 ORBSCAN