VIKY
Laparoscope, General & Plastic Surgery
ENDOCONTROL
The following data is part of a premarket notification filed by Endocontrol with the FDA for Viky.
Pre-market Notification Details
| Device ID | K082233 |
| 510k Number | K082233 |
| Device Name: | VIKY |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | ENDOCONTROL 5 Avenue Du Grand Sablon La Tronche, FR 38700 |
| Contact | Carine Huguel |
| Correspondent | Carine Huguel ENDOCONTROL 5 Avenue Du Grand Sablon La Tronche, FR 38700 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-07 |
| Decision Date | 2008-12-18 |
| Summary: | summary |
Trademark Results [VIKY]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VIKY 90546773 not registered Live/Pending |
ENDOCONTROL 2021-02-25 |
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