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VISCOAT VISCOELASTIC SOLUTION

FDA premarket approval P840064/S019 · decided 1998-03-17

Approval details

PMA number
P840064
Supplement
S019
Supplement type
Normal 180 Day Track
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VISCOAT VISCOELASTIC SOLUTION
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Alcon Laboratories
Date received
1996-12-04
Decision date
1998-03-17
Days to decision
468 days
Decision code
APPR
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR THE INCORPORATION OF VISCOAT AND PROVISC, WHICH MAKE UP THE DUOVISC PRODUCT, INTO A SINGLE PLASTIC TRAY, TO BE STERILIZED AND PROCESSED AT ALCON'S PUERTO RICO FACILITY; AND A CHANGE IN THE STERILIZATION PROCESS AT ALCON'S PUERTO RICO FACILITY FOR THE DUOVISC SYSTEM.

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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