VITAPEN
Device, Medical Examination, Ac Powered
VITAJET CORP.
The following data is part of a premarket notification filed by Vitajet Corp. with the FDA for Vitapen.
Pre-market Notification Details
| Device ID | K924447 |
| 510k Number | K924447 |
| Device Name: | VITAPEN |
| Classification | Device, Medical Examination, Ac Powered |
| Applicant | VITAJET CORP. 27075 CABOT RD. SUITE 102 Laguna Hills, CA 92653 |
| Contact | Sergio Landau |
| Correspondent | Sergio Landau VITAJET CORP. 27075 CABOT RD. SUITE 102 Laguna Hills, CA 92653 |
| Product Code | KZF |
| CFR Regulation Number | 880.6320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-01 |
| Decision Date | 1993-09-27 |
Trademark Results [VITAPEN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VITAPEN 88284010 not registered Live/Pending |
Bidjaan Kassam 2019-01-31 |
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