FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VisuMax Femtosecond Laser

K Number: K173371 · Decision Apr 13, 2018
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
82
Applicant Total
29
Review Days
168

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Basic Information

Device Name
VisuMax Femtosecond Laser
K Number
K173371
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4370
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss Meditec, Inc.
Date Received
October 27, 2017
Decision Date
April 13, 2018
Product Code
HNO
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
HNO Keratome, Ac-Powered

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Other Clearances by Carl Zeiss Meditec, Inc.

K Number Device Name
K243878 CLARUS (700)
K233933 CIRRUS™ HD-OCT Model 6000
K230350 VISULAS yag
K231075 Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)
K222200 CIRRUS HD-OCT
K191194 CLARUS
K181534 CIRRUS HD-OCT
K181444 CLARUS
K182318 Retina Workplace
K161194 PLEX Elite 9000 SS-OCT
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