# K143757: ANUTRA Feedback Aspiration Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Anutra Medical, Inc.
- Decided: Jan 8, 2015 after 8 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K980987 (1998). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110771: BD Single Use, Hypodermic Syringe, Becton, Dickinson and Company (2011) Summary page 5.

## Most influential descendants
- K201816: Arthrotap (2020), 1 descendant of its own
- K231900: A-TAP (previously called Arthrotap) (2023), 0 descendants of its own

## Indications for use
The ANUTRA Feedback Aspiration Syringe is intended for use by healthcare professionals for general purpose fluid aspiration/injection.

Source page: https://510kreport.com/device/K143757
Methodology: https://510kreport.com/methodology