POSTERIOR & ANTERIOR CHAMBER POLYMETHYLMETHACRYLATE INTRAOCULAR LENS

FDA Premarket Approval P850059 S016

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DevicePOSTERIOR & ANTERIOR CHAMBER POLYMETHYLMETHACRYLATE INTRAOCULAR LENS
Generic NameIntraocular Lens
ApplicantBAUSCH & LOMB SURGICAL, INC.1400 N. Goodman St.rochester, NY 14609 PMA NumberP850059 Supplement NumberS016 Date Received10/31/1995 Decision Date05/01/1996 Withdrawal Date 11/26/2008 Product Code HQL  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No
Date Received1995-10-31
Decision Date1996-05-01
PMAP850059
SupplementS016
Product CodeHQL 
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination ProductNo
Applicant AddressBAUSCH & LOMB SURGICAL, INC.
1400 N. Goodman St.
rochester, NY 14609 PMA NumberP850059 Supplement NumberS016 Date Received10/31/1995 Decision Date05/01/1996 Withdrawal Date 11/26/2008 Product Code HQL  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No Combination ProductNo Approval Order Statement  
APPROVAL OF THE FOLLOWING:IMPLEMENTATION OF NEW MANUFACTURING PROCESSES OF CLEAR AND VIOLET HAPTIC POLYMETHYLMETHACRYLATE (PMMA) ONE-PIECE POSTERIOR CHAMBER LENSES; THE USE OF A NEW TUMBLING PROCESS FOR YOUR THREE-PIECE LENSES; AND THE INTRODUCTION OF SEVERAL TIER A POSTERIOR CHAMBER LENSES, MODELS 8192B, 8490B, 8492B, 8090B, 8091B, 8193B, 8491B, 8493B, 8491B, 8493B, 8990B, 8991B, 8093B, 8095B, 8195B, AND 8594B

Supplemental Filings

Supplement NumberDateSupplement Type
P850059Original Filing
S024 2003-06-11 Real-time Process
S023 1999-09-21 Normal 180 Day Track
S022 1999-08-16 Normal 180 Day Track
S021 1999-02-17 Normal 180 Day Track
S020 1999-02-10 Real-time Process
S019 1998-12-23 Real-time Process
S018 1998-10-29 135 Review Track For 30-day Notice
S017 1998-08-07 Normal 180 Day Track
S016 1995-10-31 Normal 180 Day Track
S015
S014 1989-12-20 Normal 180 Day Track
S013 1989-09-08 Normal 180 Day Track
S012 1989-01-11 Normal 180 Day Track
S011 1988-12-28 Normal 180 Day Track
S010 1988-12-21 Normal 180 Day Track
S009 1988-12-19 Normal 180 Day Track
S008 1988-08-22 Special (immediate Track)
S007 1988-05-17 Normal 180 Day Track
S006 1988-01-07 Special (immediate Track)
S005 1987-12-14 Normal 180 Day Track
S004
S003
S002
S001 1987-02-20 Normal 180 Day Track

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.