FDA 510(k) Applications Submitted by BETH A ROBERTS

FDA 510(k) Number Submission Date Device Name Applicant
K992374 07/15/1999 AURORA HL PREMIER LASER SYSTEMS, INC.
K992620 08/05/1999 BLULAZE PREMIER LASER SYSTEMS, INC.
K993285 09/30/1999 AURORA SL PREMIER LASER SYSTEMS, INC.


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