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Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack

FDA premarket approval P810031/S075 · decided 2024-04-15

Approval details

PMA number
P810031
Supplement
S075
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD), Healon Duet PRO Dual Pack
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2024-01-18
Decision date
2024-04-15
Days to decision
88 days
Decision code
APPR
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
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

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