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

DISCON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR

K Number: K051129 · Decision Aug 12, 2005
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
11
Review Days
101

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Basic Information

Device Name
DISCON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR
K Number
K051129
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innova Vision, Inc.
Date Received
May 3, 2005
Decision Date
August 12, 2005
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

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Other Clearances by Innova Vision, Inc.

K Number Device Name
K240519 Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft Contact Lens
K232139 Innova Vision (inifilcon A) Silicone Hydrogel Soft (Hydrophilic) Contact Lens
K222954 Innova Vision Hydrogel (Etafilcon A) Soft (Hydrophilic) Contact Lens
K213119 Innova Vision Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact Lens
K112373 CALAVIEW COLOR (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR MODIFICATION
K083288 DISCON PLUS (ETAFILCON A) CONTACT LENS VISIBILITY TINT WITH UV BLOCKER
K073060 CALAVIEW (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR
K062541 CALAVIEW COLORS (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS
K053191 DISCON DAILY (ETAFILCON A) ONE-DAY SOFT (HYDROPHILIC) CONTACT LENS
K033136 I-LUX INNOVA BLUE TINT LENS, MODEL SUPER O2
Search all 11 clearances from Innova Vision, Inc. →