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PERFLUORON OCULAR ENDOTAMPONADE

FDA premarket approval P950018/S016 · decided 2013-07-09

Approval details

PMA number
P950018
Supplement
S016
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PERFLUORON OCULAR ENDOTAMPONADE
Generic name
Fluid, intraocular
Applicant
Alcon Laboratories
Date received
2012-11-08
Decision date
2013-07-09
Days to decision
243 days
Decision code
APPR
Product code
LWL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR CHANGES TO THE ADHESIVE RESINS (LIMONENE-BASED RESIN TR7125 HAS REPLACED THE CURRENT LIMONENE-BASED RESIN TR1135, AND ETHYLENE VINYL ACETATE RESIN UL8705 HAS REPLACED THE CURRENT EVA RESIN 205W) USED FOR THE TYVEK LID AND VALIDATION OF AN AIR-OVER-STEAM (AOS) STERILIZATION CYCLE TO ALIGN PRACTICES AMONG PRODUCTS WITHIN THE MANUFACTURING FACILITY.

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510(k) clearances by this applicant

RecordFirmDate
NEXT GENERATION LASER (K062624)Alcon Laboratories2007-11-05
SMALL VOLUME SYRINGE (K062865)Alcon Laboratories2007-08-23
RGP MULTI-PURPOSE SOLUTION ID 100136 (K000148)Alcon Laboratories2000-04-11
OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP (K984573)Alcon Laboratories1999-09-16
OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER (K990480)Alcon Laboratories1999-05-10
MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 (K984575)Alcon Laboratories1999-01-14
OPTI-ONE MULTI-PURPOSE SOLUTION (K983973)Alcon Laboratories1998-12-18
MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 (K983780)Alcon Laboratories1998-12-18