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CELLUGEL OPHTHALMIC VISCOSURGICAL DEVICE

FDA premarket approval P990023/S005 · decided 2008-11-26

Approval details

PMA number
P990023
Supplement
S005
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CELLUGEL OPHTHALMIC VISCOSURGICAL DEVICE
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Alcon Laboratories
Date received
2008-10-31
Decision date
2008-11-26
Days to decision
26 days
Decision code
OK30
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
USE OF A NEW INDUSTRIAL DISINFECTANT FOR THE DISINFECTION OF CLEANROOMS USED DURING THE PRODUCTION PROCESS.

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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