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PERFLUORON

FDA premarket approval P950018/S009 · decided 2003-03-20

Approval details

PMA number
P950018
Supplement
S009
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PERFLUORON
Generic name
Fluid, intraocular
Applicant
Alcon Laboratories
Date received
2003-02-14
Decision date
2003-03-20
Days to decision
34 days
Decision code
APPR
Product code
LWL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR A NEW STABILITY PROTOCOL THAT WILL EXTEND THE EXPIRATION DATING FOR PERFLUORON FROM 2 YEARS TO UP TO 4 YEARS FOR THE CURRENTLY APPROVED PRODUCT CONFIGURATION, WITH STABILITY TESTING DATA REPORTED VIA ANNUAL REPORTS IN THE FUTURE.

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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