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FOCUS NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES

FDA premarket approval P010019 · decided 2001-10-11

Approval details

PMA number
P010019
Trade name
FOCUS NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES
Generic name
Lenses, soft contact, extended wear
Applicant
Alcon Laboratories, Inc.
Date received
2001-03-21
Decision date
2001-10-11
Days to decision
204 days
Decision code
APPR
Product code
LPM
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR THE FOCUS NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES FOR EXTENDED WEAR. THE DEVICE WILL BE MARKETED WITH THE FOLLOWING TRADE NAMES AND INDICATIONS: FOCUS NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES ARE INDICATED FOR THE OPTICAL CORRECTION OF REFRACTIVE AMETROPIA (MYOPIA AND HYPEROPIA) IN PHAKIC OR APHAKIC PERSONS WITH NON-DISEASED EYES AND WITH UP TO APPROXIMATELY 1.50 DIOPTERS OF ASTIGMATISM. FOCUS NIGHT AND DAY TORIC (LOTRAFILCON A) SOFT CONTACT LENSES ARE INDICATED F

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510(k) clearances by this applicant

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