# K231900: A-TAP (previously called Arthrotap)

- Pathway: 510(k) (Special)
- Applicant: Elcam Medical Acal
- Decided: Jul 25, 2023 after 27 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: 4 generations back to K980987 (1998). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201816: Arthrotap, Accuro Technologies, Inc. (2020) Summary page 4.

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

Source page: https://510kreport.com/device/K231900
Methodology: https://510kreport.com/methodology