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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DevicePOSTERIOR CHAMBER IOL'S
Generic Nameintraocular lens
Regulation Number886.3600
ApplicantBausch & Lomb
1400 N. Goodman St.
Rochester, NY 14609
PMA NumberP790027
Supplement NumberS062
Date Received12/23/1998
Decision Date01/28/1999
Withdrawal Date11/26/2008
Product Code HQL 
Advisory Committee Ophthalmic
Supplement TypeReal-Time Process
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for an alternate packaging configuration for the PMMA IOLs, manufactured at Claremont, CA facility.
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