Atlas FDA

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

FDA premarket approval P960011/S020 · decided 2012-01-27

Approval details

PMA number
P960011
Supplement
S020
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BVI 1% OVD (1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Altacor , Ltd.
Date received
2011-12-29
Decision date
2012-01-27
Days to decision
29 days
Decision code
OK30
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Theale
Statement
NEW VISCOMETER, FOR THE IN-PROCESS AND QUALITY CONTROL RELEASE TESTING.

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