MEDIVAX
Injector, Fluid, Non-electrically Powered
VITAJET CORP.
The following data is part of a premarket notification filed by Vitajet Corp. with the FDA for Medivax.
Pre-market Notification Details
| Device ID | K945548 |
| 510k Number | K945548 |
| Device Name: | MEDIVAX |
| Classification | Injector, Fluid, Non-electrically Powered |
| Applicant | VITAJET CORP. 27075 CABOT RD. SUITE 102 Laguna Hills, CA 92653 |
| Contact | Serfio Landau |
| Correspondent | Serfio Landau VITAJET CORP. 27075 CABOT RD. SUITE 102 Laguna Hills, CA 92653 |
| Product Code | KZE |
| CFR Regulation Number | 880.5430 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-11-14 |
| Decision Date | 1995-11-20 |
Trademark Results [MEDIVAX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MEDIVAX 74370723 1889210 Dead/Cancelled |
Vitajet Corporation 1993-03-22 |
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