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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 NameCHIROFLEX MODELS 32 C10XX SILICONE POSTERIOR IOL
Classification Nameintraocular lens
Generic Namechiroflex models 32 c10xx silicone posterior iol
Regulation Number886.3600
ApplicantBAUSCH & LOMB, INC.
PMA NumberP910058
Date Received09/23/1991
Decision Date01/17/1992
Withdrawal Date 09/17/2010
Product Code
HQL[ Registered Establishments with HQL ]
Docket Number 92M-0046
Notice Date 02/18/1992
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S005 S007 S008 S009 S010 S011 
S012 
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