AbbVie PEG
FDA 510(k) clearance K142793 · decided 2015-01-14
Clearance details
- K-number
- K142793
- Device name
- AbbVie PEG
- Applicant
- AbbVie , Inc.
- Decision
- Unknown
- Date received
- 2014-09-26
- Decision date
- 2015-01-14
- Days to decision
- 110 days
- Clearance type
- Traditional
- Product code
- KNT
- Device class
- 2
- Regulation number
- 876.5980
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- North Chicago, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch AbbVie
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.