CRYSTALENS SALINE SPRAY

FDA Premarket Approval P850065 S008

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

DeviceCRYSTALENS SALINE SPRAY
Generic NameAccessories, Soft Lens Products
ApplicantSTERICON, INC.
Date Received1987-03-19
Decision Date1987-08-17
PMAP850065
SupplementS008
Product CodeLPN 
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonLocation Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address STERICON, INC. 19742 Macarthur Blvd. suite 235 irvine, CA 92715

Supplemental Filings

Supplement NumberDateSupplement Type
P850065Original Filing
S013 1990-06-22 Normal 180 Day Track
S012 1988-03-15 Normal 180 Day Track
S011
S010
S009 1987-10-13 Normal 180 Day Track
S008 1987-03-19 Normal 180 Day Track
S007 1987-03-19 Normal 180 Day Track
S006 1987-03-18 Normal 180 Day Track
S005
S004
S003
S002 1986-07-03 Normal 180 Day Track
S001

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