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

CONTAFLEX GM3 58% (ACOFILCON A) SPHERICAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, LATHE-CUT)

K Number: K023349 · Decision Dec 24, 2002
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
485
Applicant Total
18
Review Days
78

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Basic Information

Device Name
CONTAFLEX GM3 58% (ACOFILCON A) SPHERICAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, LATHE-CUT)
K Number
K023349
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Contamac, Ltd.
Date Received
October 7, 2002
Decision Date
December 24, 2002
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 Contamac, Ltd.

K Number Device Name
K212631 Optimum Infinite (tisilfocon A) Daily Wear Contact Lenses
K182304 Hyper GP (tisilfocon A) Daily Wear Contact Lens
K181566 Nutrifill
K180616 OPTIMUM GP (roflufocon D, roflurocon E) Daily Wear Contact Lens, HEXA100 (hexafocon A) Daily Wear Contact Lens
K171575 ENFLU 18 (enflufocon A) Daily Wear Contact Lens
K171077 HEXA100 (hexafocon A) Daily Wear Contact Lenses
K161100 Optimum GP with HPT (roflufocon A, B, C, D, and E) Daily Wear Contact Lenses
K160859 OPTIMUM GP OK Daily Wear Contact Lens (roflufocon D & E)
K150590 CONTAFLEX 54 (hioxifilcon D) Spherical Soft Contact Lens for Daily Wear, CONTAFLEX 49 (hioxifilcon B) Spherical Soft Contact Lens for Daily Wear,
K081178 OPTIMUM HR-1.51 (HIFLUFOCON A) AND HR-1.53 (HIFLUFOCON B) DAILY WEAR CONTACT LENSES
Search all 18 clearances from Contamac, Ltd. →