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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 NameBIOLON 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID
Classification Nameaid, surgical, viscoelastic
Generic Nameviscoelastic opthalmo-surgical aid agent
Regulation Number886.4275
ApplicantBIO-TECHNOLOGY GENERAL CORP.
PMA NumberP960011
Supplement NumberS001
Date Received08/31/1998
Decision Date09/09/1998
Product Code
LZP[ Registered Establishments with LZP ]
Advisory Committee Ophthalmic
Supplement Typenormal 180 day track
Supplement Reason location change: distributor
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for akorn, inc. To distribute biolon(tm) in the united states.
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