Abb Vie J
by Abbvie Inc.
510(k) K133096
Abb Vie J is a medical device (FDA Class II; FDA product code KNT, Tubes, Gastrointestinal (And Accessories)) made by Abbvie Inc., cleared under FDA 510(k) K133096 on 18 Jun 2014, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK133096 | Date18 Jun 2014 | StatusActive |
Official records
- FDA 510(k) database K133096
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KNT
- FDA applicant
- AbbVie , Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 876.5980
- Advisory committee
- Gastroenterology, Urology
- FDA decision
- SESE Substantially Equivalent
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