# K082870: Vti Intraoperative Doppler Systems

- Pathway: 510(k) (Special)
- Applicant: Vascular Technology Incorporated
- Decided: Oct 28, 2008 after 29 days
- Product code: DPW (Flowmeter, Blood, Cardiovascular)
- Device class: 2
- Regulation: 21 CFR 870.2100
- Recalls of this device: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K212065: VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (2021), 3 descendants of its own
- K211589: VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (2022), 2 descendants of its own
- K241583: VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01) (2024), 1 descendant of its own
- K260700: BlueDop Vascular Expert (2026), 0 descendants of its own
- K251904: VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01) (2025), 0 descendants of its own

## Recalls of this device
- May 28, 2014 · Class II · Z-2000-2014: Report of the product penetrating the sterile barrier; this could render the product unsterile.
- May 28, 2014 · Class II · Z-1998-2014: Report of the product penetrating the sterile barrier; this could render the product unsterile.
- May 28, 2014 · Class II · Z-1999-2014: Report of the product penetrating the sterile barrier; this could render the product unsterile.
- May 28, 2014 · Class II · Z-2001-2014: Report of the product penetrating the sterile barrier; this could render the product unsterile.

## Indications for use
The VTI Intraoperative Doppler Systems are intended for the intraoperative and transcutaneous evaluation of blood flow. Indications for Use form filed with the FDA for the VTI Doppler Probes lists the clinical applications as Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.

Source page: https://510kreport.com/device/K082870
Methodology: https://510kreport.com/methodology