FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lenses, Soft Contact, Extended Wear

PMA: P010019 · Supplement: S006 · Decision Jul 26, 2007
Classifications
1
FEI Numbers
56
Registration Numbers
56

Basic Information

Device Name
Lenses, Soft Contact, Extended Wear
Trade Name
NIGHT & DAY (LOTRAFILCON A) SOFT CONTACT LENSES FOR UP TO 30 NIGHTS CONTINUOUS WEAR
PMA Number
P010019
Supplement Number
S006
Device Class
FDA Class 3
Product Code
LPM
Generic Name
Lenses, soft contact, extended wear
Regulation Number
886.5925
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
July 26, 2007
Date Received
April 2, 2007
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR REVISED LABELING FOR NIGHT & DAY (LOTRAFILCON A) SOFT CONTACT LENSES FOR UP TO 30 NIGHTS CONTINUOUS WEAR.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LPM Lenses, Soft Contact, Extended Wear