SYNSOFT(TM) (POLYMACON) BIFOCAL CONTACT LENS

FDA Premarket Approval P840006 S005

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

DeviceSYNSOFT(TM) (POLYMACON) BIFOCAL CONTACT LENS
Generic NameLenses, Soft Contact, Daily Wear
ApplicantSALVATORI OPHTHALMICS MFG. CORP.
Date Received1990-10-02
Decision Date1991-04-24
PMAP840006
SupplementS005
Product CodeLPL 
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonLocation Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address SALVATORI OPHTHALMICS MFG. CORP. 6416 Parkland Dr. sarasota, FL 34243

Supplemental Filings

Supplement NumberDateSupplement Type
P840006Original Filing
S006 1990-10-15 Normal 180 Day Track
S005 1990-10-02 Normal 180 Day Track
S004 1990-08-02 Normal 180 Day Track
S003
S002 1985-02-27
S001 1985-02-25

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.