FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

SAUFLON 55 UV SOFT (HYDROPHILIC) CONTACT LENS

K Number: K013649 · Decision Dec 26, 2001
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
12
Review Days
51

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Basic Information

Device Name
SAUFLON 55 UV SOFT (HYDROPHILIC) CONTACT LENS
K Number
K013649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sauflon Pharmaceuticals, Ltd.
Date Received
November 5, 2001
Decision Date
December 26, 2001
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

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Other Clearances by Sauflon Pharmaceuticals, Ltd.

K Number Device Name
K133740 SAUFLON CLARITI WITH TINT, SAUFLON CLARITI TORIC WITH TINT, SAUFLON CLARITI MULTIFOCAL WITH TINT
K130342 SAUFLON CLARITI (SOMOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER
K130331 SAUFLON CLARITI 1 DAY (SOMOFILCON A) SOFT (HYDROPHILIC) DAILY DISPOSABLE CONTACT LENS WITH UV BLOCKER
K130734 SAUFLON MULTIPURPOSE SOLUTION
K052832 SAUFLON NEW DAY (METHAFILCON A) SOFT (HYDROPHILIC) DAILY DISPOSABLE CONTACT LENSES
K052809 SAUFLON FLAT COLOURED LENS CASE
K033656 SAUFLON FLAT LENS CASE/SAUFLON 2003 BARREL LENS CASE
K030278 SAUFLON MULTIPURPOSE SOLUTION - NO RUB
K010559 SAUFLON MULTI LENS CARE SYSTEM
K011456 DELTA PLUS MULTIACTION SOLUTION FOR RIGID GAS PERMEABLE CONTACT LENSES
Search all 12 clearances from Sauflon Pharmaceuticals, Ltd. →