PMA P180035S024

Device
MiSight 1 Day (omafilcon A)
Applicant
CooperVision, Inc.
PMA number
P180035
Supplement
S024
Product code
QIT
Decision date
2024-10-07
Classification
Ophthalmic
Generic name
Daily wear soft contact lens to reduce the progression of myopia
Approval order statement
relocation of a secondary packaging line within the CooperVision, Inc. facility in West Henrietta, New York

Current openFDA PMA Record#

Device
MiSight 1 Day (omafilcon A)
Applicant
CooperVision, Inc.
PMA number
P180035
Supplement
S024
Product code
QIT
Generic name
Daily wear soft contact lens to reduce the progression of myopia
Decision date
2024-10-07
Decision code
OK30
Date received
2024-09-23
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
relocation of a secondary packaging line within the CooperVision, Inc. facility in West Henrietta, New York