Atlas FDA

PERFLUORON

FDA premarket approval P950018/S004 · decided 2000-06-15

Approval details

PMA number
P950018
Supplement
S004
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PERFLUORON
Generic name
Fluid, intraocular
Applicant
Alcon Laboratories
Date received
2000-02-17
Decision date
2000-06-15
Days to decision
119 days
Decision code
APPR
Product code
LWL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR THE FILTER STERILIZATION AND ASEPTIC FILL FACILITY LOCATED AT CHESAPEAKE BIOLOGICAL LABORATORIES (CBL), IND., BALTIMORE, MARYLAND 21230.

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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