PMA P810031S075

Device
Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack
Applicant
Johnson & Johnson Surgical Vision, Inc.
PMA number
P810031
Supplement
S075
Product code
LZP
Decision date
2024-04-15
Classification
Ophthalmic
Generic name
AID, SURGICAL, VISCOELASTIC
Approval order statement
approval of an alternative elastomeric plunger stopper used in the primary closure configuration for the Healon EndoCoat Ophthalmic Viscosurgical Device (OVD) (3% Sodium Hyaluronate), and Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack

Current openFDA PMA Record#

Device
Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack
Applicant
Johnson & Johnson Surgical Vision, Inc.
PMA number
P810031
Supplement
S075
Product code
LZP
Generic name
AID, SURGICAL, VISCOELASTIC
Decision date
2024-04-15
Decision code
APPR
Date received
2024-01-18
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Approval order statement
approval of an alternative elastomeric plunger stopper used in the primary closure configuration for the Healon EndoCoat Ophthalmic Viscosurgical Device (OVD) (3% Sodium Hyaluronate), and Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack