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FDA 510(k) Applications Submitted by LORNA K LINVILLE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990043
01/06/1999
SMOOTHLASE ALEXANDRITE LASER SYSTEM
LEISEGANG MEDICAL, INC.
K121890
06/28/2012
GENESYS PRESSFT SUTURE ANCHOR
LINVATEC CORPORATION D/B/A CONMED LINVATEC
K982316
07/02/1998
LASEAWAY ALEXANDRITE LASER SYSTEM
SILVER CREEK, INC.
K092898
09/21/2009
CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES
CONMED LINVATEC
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