# K093915: Deka Tac Device

- Pathway: 510(k) (Traditional)
- Applicant: Deka Research & Development Corp.
- Decided: Aug 23, 2011 after 609 days
- Product code: FIG (Clamp, Tubing, Blood, Automatic)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K914459 (1992). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K914459: Automatic Tubing Clamp, Rocky Mountain Research, Inc. (1992) Summary page 1.
- K010888: Sideport Pinch Clamp Device, Medivice Systems, Ltd. (2001) Summary page 1.

## Indications for use
The DEKA TAG is an automatic tubing clamp device intended for use in a clinical facility as an accessory to a hemodialysis blood circuit to automatically clamp the blood flow in the hemodialysis circuit upon detection of tension in the venous access line in excess of a pre-defined threshold value. The DEKA TAG may be mounted on, or removed from, already assembled hemodialysis blood circuits.

Source page: https://510kreport.com/device/K093915
Methodology: https://510kreport.com/methodology