The following data is part of a premarket notification filed by Abbvie Inc. with the FDA for Abb Vie J.
| Device ID | K133096 |
| 510k Number | K133096 |
| Device Name: | ABB VIE J |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | ABBVIE INC. 1 N. WAUKEGAN RD. North Chicago, IL 60064 |
| Contact | Katherine Wortley |
| Correspondent | Katherine Wortley ABBVIE INC. 1 N. WAUKEGAN RD. North Chicago, IL 60064 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-30 |
| Decision Date | 2014-06-18 |
| Summary: | summary |