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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameMODEL 91-50 IOL
Classification Nameintraocular lens
Generic Nameanterior chamber iol
Regulation Number886.3600
ApplicantBAUSCH & LOMB, INC.
PMA NumberP820044
Date Received07/12/1982
Decision Date12/27/1985
Withdrawal Date 04/06/2009
Product Code
HQL[ Registered Establishments with HQL ]
Docket Number 86M-0032
Notice Date 02/14/1986
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 
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