PMA P880010S019

Device
Posterior Chamber Intraocular Lens
Applicant
ALCON LABORATORIES
PMA number
P880010
Supplement
S019
Decision date
1998-09-04

Current openFDA PMA Record

Device
POSTERIOR CHAMBER INTRAOCULAR LENS
Applicant
Alcon Laboratories
PMA number
P880010
Supplement
S019
Product code
HQL
Generic name
intraocular lens
Decision date
1998-09-04
Decision code
APPR
Date received
1996-08-08
Supplement type
Normal 180 Day Track
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Approval for an alternate sterilization process using 100% ethylene oxide, an alternate microbioloigcal monitoring system and one resterilization in the event of an "aborted cycle."

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