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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameMODELS PC10 & PC21
Classification Nameintraocular lens
Generic Nameposterior chamber iol
Regulation Number886.3600
ApplicantAMERICAN MEDICAL OPTICS
PMA NumberP820049
Supplement NumberS008
Date Received03/28/1986
Decision Date09/24/1986
Product Code
HQL[ Registered Establishments with HQL ]
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
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