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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