Atlas FDA

BD 1% OVD ( 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)

FDA premarket approval P960011/S016 · decided 2010-01-07

Approval details

PMA number
P960011
Supplement
S016
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BD 1% OVD ( 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Altacor , Ltd.
Date received
2009-12-07
Decision date
2010-01-07
Days to decision
31 days
Decision code
OK30
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Theale
Statement
CHANGE IN A QUALITY CONTROL TEST METHOD FOR THE FINISHED DEVICE.

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