The following data is part of a premarket notification filed by Vomaris Innovations Inc. with the FDA for Procellera.
| Device ID | K130350 |
| 510k Number | K130350 |
| Device Name: | PROCELLERA |
| Classification | Dressing, Wound, Drug |
| Applicant | VOMARIS INNOVATIONS INC. 3100 W. Ray Rd, Ste 148 Chandler, AZ 85226 |
| Contact | Mary Maijer |
| Correspondent | Jeffry Skiba VOMARIS INNOVATIONS INC. 3100 W. Ray Rd, Ste 148 Chandler, AZ 85226 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-02-12 |
| Decision Date | 2013-07-02 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROCELLERA 77510397 not registered Dead/Abandoned |
VOMRAIS INNOVATIONS, INC. 2008-06-27 |
![]() PROCELLERA 77510370 3873875 Live/Registered |
VOMARIS INNOVATIONS, INC. 2008-06-27 |
![]() PROCELLERA 77510270 4444012 Live/Registered |
VOMARIS INNOVATIONS, INC. 2008-06-27 |