The following data is part of a premarket notification filed by Inmed Corp. with the FDA for Cantor Tube.
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CANTOR TUBE 71622429 0571628 Dead/Expired |
CLAY-ADAMS COMPANY, INC. 1951-12-13 |