Atlas FDA

SILIKON 1000

FDA premarket approval P950008/S010 · decided 2013-07-15

Approval details

PMA number
P950008
Supplement
S010
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
SILIKON 1000
Generic name
Fluid, intraocular
Applicant
Alcon
Date received
2013-06-11
Decision date
2013-07-15
Days to decision
34 days
Decision code
APPR
Product code
LWL
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
APPROVAL FOR LABELING MODIFICATIONS TO THE SILIKON 1000 OIL DIRECTIONS FOR USE.

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510(k) clearances by this applicant

RecordFirmDate
ALCON VISION SYSTEM (K063583)Alcon2008-05-09
OPTI-FREE EXPRESS MULTI-PURPOSE SOLUTION (K981574)Alcon1998-07-06