# K201816: Arthrotap

- Pathway: 510(k) (Traditional)
- Applicant: Accuro Technologies, Inc.
- Decided: Oct 16, 2020 after 107 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: 3 generations back to K980987 (1998). 3 ancestors in all.
1 later device descends 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)
- K143757: ANUTRA Feedback Aspiration Syringe, Anutra Medical, Inc. (2015) Summary page 4.

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

## Indications for use
The ARTHROTAP is intended for use by healthcare professionals for general purpose fluid aspiration/injection.

Source page: https://510kreport.com/device/K201816
Methodology: https://510kreport.com/methodology