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

Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens

K Number: K160803 · Decision Jul 13, 2016
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
97
Review Days
112

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Basic Information

Device Name
Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens
K Number
K160803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CooperVision, Inc.
Date Received
March 23, 2016
Decision Date
July 13, 2016
Product Code
LPL
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
LPL Lenses, Soft Contact, Daily Wear

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LPL), ordered by most recent decision date.

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Other Clearances by CooperVision, Inc.

K Number Device Name
K234127 Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker
K220070 MyDay (stenfilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens, Avaira Vitality (fanfilcon A) Soft (Hydrophilic) Contact Lens
K213164 Avaira Vitality
K202756 Clariti 1 Day (somofilcon A), Clariti 1 Day Toric (somofilcon A), Clariti 1 Day Multifocal (somofilcon A), Clariti 1 Day Multifocal Toric (somofilcon A)
K191763 MyDay (Stenfilcon A) ASPHERE, MyDay (Stenfilcon A) TORIC, MyDay (Stenfilcon A) MULTIFOCAL, MyDay (Stenfilcon A) MULTIFOCAL TORIC
K190965 MyDay
K181920 Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker
K133627 AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS
K131378 SUS (STENFILCON A) CONTACT LENS
K123202 PROCLEAR (OMAFILCON A) SOFT HYDROPHILIC) CONTACT LENS
Search all 97 clearances from CooperVision, Inc. →