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

OPTIMUS FUSION: SLT, YAG AND YAG/SLT

K Number: K140336 · Decision Jun 25, 2014
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
30
Review Days
135

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Basic Information

Device Name
OPTIMUS FUSION: SLT, YAG AND YAG/SLT
K Number
K140336
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quantel Medical
Date Received
February 10, 2014
Decision Date
June 25, 2014
Product Code
HQF
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
HQF Laser, Ophthalmic

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