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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.
 
DeviceEN VISTA HYDROPHOBIC ACRYLIC INTRAOCULAR LENS
Classification Nameintraocular lens
Generic Nameintraocular lens
Regulation Number886.3600
Applicant
Bausch & Lomb, Inc.
50 technology drive
irvine, CA 92618
PMA NumberP910056
Supplement NumberS013
Date Received09/07/2012
Decision Date10/19/2012
Product Code
HQL[ Registered Establishments with HQL ]
Advisory Committee Ophthalmic
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for changes to the directions for use (dfu) to specify that the envista mx60 lens is approved for use with the medicel accuject 2. 2 (rev. 1) injector set,or other injector sets that specifically identify the envista mx60 lens in the cleared labeling.
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