MENICON SF-P
Lens, Contact (other Material) - Daily
MENICON CO. LTD.
The following data is part of a premarket notification filed by Menicon Co. Ltd. with the FDA for Menicon Sf-p.
Pre-market Notification Details
| Device ID | K000233 |
| 510k Number | K000233 |
| Device Name: | MENICON SF-P |
| Classification | Lens, Contact (other Material) - Daily |
| Applicant | MENICON CO. LTD. 269A BALLARDVALE ST. Wilmington, MA 01887 |
| Contact | Beverley D Venuti |
| Correspondent | Beverley D Venuti MENICON CO. LTD. 269A BALLARDVALE ST. Wilmington, MA 01887 |
| Product Code | HQD |
| CFR Regulation Number | 886.5916 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-01-27 |
| Decision Date | 2000-05-19 |
Trademark Results [MENICON SF-P]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MENICON SF-P 74275852 1874528 Dead/Cancelled |
Menicon Co., Ltd. 1992-05-15 |
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