CANTOR TUBE
Tubes, Gastrointestinal (and Accessories)
INMED CORP.
The following data is part of a premarket notification filed by Inmed Corp. with the FDA for Cantor Tube.
Pre-market Notification Details
| Device ID | K841039 |
| 510k Number | K841039 |
| Device Name: | CANTOR TUBE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | INMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-03-12 |
| Decision Date | 1984-04-13 |
Trademark Results [CANTOR TUBE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CANTOR TUBE 71622429 0571628 Dead/Expired |
CLAY-ADAMS COMPANY, INC. 1951-12-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.