PRO-VIT
Instrument, Vitreous Aspiration And Cutting, Ac-powered
M. IMONTI AND ASSOCIATES INC.,
The following data is part of a premarket notification filed by M. Imonti And Associates Inc., with the FDA for Pro-vit.
Pre-market Notification Details
| Device ID | K950799 |
| 510k Number | K950799 |
| Device Name: | PRO-VIT |
| Classification | Instrument, Vitreous Aspiration And Cutting, Ac-powered |
| Applicant | M. IMONTI AND ASSOCIATES INC., 25707 COMPASS WAY San Juan Capistrano, CA 92675 |
| Contact | Maurice Imonti |
| Correspondent | Maurice Imonti M. IMONTI AND ASSOCIATES INC., 25707 COMPASS WAY San Juan Capistrano, CA 92675 |
| Product Code | HQE |
| CFR Regulation Number | 886.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-21 |
| Decision Date | 1995-04-28 |
Trademark Results [PRO-VIT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRO-VIT 75130390 2077432 Dead/Cancelled |
M. Imonti & Associates 1996-07-05 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.