NEVOSCOPE
Device, Medical Examination, Ac Powered
NIZAR A. MULLANI
The following data is part of a premarket notification filed by Nizar A. Mullani with the FDA for Nevoscope.
Pre-market Notification Details
| Device ID | K954943 |
| 510k Number | K954943 |
| Device Name: | NEVOSCOPE |
| Classification | Device, Medical Examination, Ac Powered |
| Applicant | NIZAR A. MULLANI 719 SANTA MARIA SUGARLAND, TX 77478 |
| Contact | NIZAR A MULLANI |
| Correspondent | NIZAR A MULLANI NIZAR A. MULLANI 719 SANTA MARIA SUGARLAND, TX 77478 |
| Product Code | KZF |
| CFR Regulation Number | 880.6320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-30 |
| Decision Date | 1996-03-27 |
Trademark Results [NEVOSCOPE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NEVOSCOPE 78716532 3236089 Live/Registered |
Translite, LLC 2005-09-20 |
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