NO-MES
Tubes, Gastrointestinal (and Accessories)
ETHOX CORP.
The following data is part of a premarket notification filed by Ethox Corp. with the FDA for No-mes.
Pre-market Notification Details
| Device ID | K935633 |
| 510k Number | K935633 |
| Device Name: | NO-MES |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | ETHOX CORP. 251 SENECA ST. Buffalo, NY 14204 |
| Contact | John A Young |
| Correspondent | John A Young ETHOX CORP. 251 SENECA ST. Buffalo, NY 14204 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-23 |
| Decision Date | 1994-09-30 |
Trademark Results [NO-MES]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NO-MES 90307891 not registered Live/Pending |
Industrial Tool & Die Co., Inc. 2020-11-09 |
 NO-MES 74410916 1956725 Dead/Cancelled |
Ethox Corp. 1993-07-12 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.