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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