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

Nutrifill

K Number: K181566 · Decision Oct 22, 2018
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
32
Applicant Total
18
Review Days
130

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Basic Information

Device Name
Nutrifill
K Number
K181566
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5918
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Contamac, Ltd.
Date Received
June 14, 2018
Decision Date
October 22, 2018
Product Code
MRC
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
MRC Products, Contact Lens Care, Rigid Gas Permeable

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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
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
K070628 OPTIMUM GP (ROFLUFOCON A,B,C,D&E) DAILY WEAR CONTACT LENS.
Search all 18 clearances from Contamac, Ltd. →