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SODIUM HYALURONATE OPHTHALMIC VISCOELASTIC DEVICES-HEALON, HEALON GV, HEALON5 PRODUCTS, HEALON ULTIMATE DUAL PACK, AND H

FDA premarket approval P810031/S055 · decided 2015-12-22

Approval details

PMA number
P810031
Supplement
S055
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
SODIUM HYALURONATE OPHTHALMIC VISCOELASTIC DEVICES-HEALON, HEALON GV, HEALON5 PRODUCTS, HEALON ULTIMATE DUAL PACK, AND H
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2015-11-25
Decision date
2015-12-22
Days to decision
27 days
Decision code
APPR
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR CHANGES MADE TO THE DIRECTIONS FOR USE (DFU).

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