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

TORIC EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) TORIC MULTIFOCAL CONTACT LENS FOR DAILY WEAR

K Number: K013467 · Decision Nov 20, 2001
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
6
Review Days
33

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Basic Information

Device Name
TORIC EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) TORIC MULTIFOCAL CONTACT LENS FOR DAILY WEAR
K Number
K013467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Soflex Contact Lens Industries , Ltd.
Date Received
October 18, 2001
Decision Date
November 20, 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

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

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Other Clearances by Soflex Contact Lens Industries , Ltd.

K Number Device Name
K033655 SOFLEX SOFT K (XYLOFILCON A) SOFT (HYDROPHILIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR
K030842 ENI-EYE Q TORIC (ACOFILCON) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR, ENI-EYE (ACOFILCON) SOFT (HYDROP
K020642 SOFT K. AND SOFT K. TORIC (XYLOFICON A) SOFT (HYDROPHILLIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR
K013469 EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR
K011256 TORIC LITE LENS