Atlas FDA

POSTERIOR CHAMBER IOL'S

FDA premarket approval P790027/S062 · decided 1999-01-28

Approval details

PMA number
P790027
Supplement
S062
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
POSTERIOR CHAMBER IOL'S
Generic name
intraocular lens
Applicant
Bausch & Lomb
Date received
1998-12-23
Decision date
1999-01-28
Days to decision
36 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Rochester, NY
Statement
Approval for an alternate packaging configuration for the PMMA IOLs, manufactured at Claremont, CA facility.

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