The following data is part of a premarket notification filed by Osyris with the FDA for Pharaon 980 Endo/exo, Osyfibre 600, Control4+ Handpiece.
Device ID | K080731 |
510k Number | K080731 |
Device Name: | PHARAON 980 ENDO/EXO, OSYFIBRE 600, CONTROL4+ HANDPIECE |
Classification | Powered Laser Surgical Instrument |
Applicant | OSYRIS 121 RUE CHANZY, BP 90140 Hellemmes , France, FR F59260 |
Contact | Jaouad Zemmouri |
Correspondent | Jaouad Zemmouri OSYRIS 121 RUE CHANZY, BP 90140 Hellemmes , France, FR F59260 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-03-14 |
Decision Date | 2008-07-17 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
03760227850150 | K080731 | 000 |