The following data is part of a premarket notification filed by Ethox Corp. with the FDA for No-mes.
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 |
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 |