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FDA 510(k) Applications Submitted by JONATHAN S KAHANM ESQ.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981677
05/12/1998
REPOSE BONE SCREW SYSTEM
INFLUENCE, INC.
DEN000008
12/19/2000
DULBECCO'S MODIFIED EAGLE MEDIUM (DMEM)
LIFE TECHNOLOGIES, INC.
K981126
03/27/1998
CERALAS G FREQUENCY DOUBLED ND: YAG LASER SYSTEMS, CERALAS G3
CERAMOPTEC, INC.
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