FDA 510(k) Applications Submitted by OSYRIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080731 | 03/14/2008 | PHARAON 980 ENDO/EXO, OSYFIBRE 600, CONTROL4+ HANDPIECE | OSYRIS |
| K082004 | 07/14/2008 | SMOOTHKIT+ | OSYRIS |
| K073617 | 12/26/2007 | PHARAON LIPO | OSYRIS |
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