SIW · Robotic Peripheral Venous Blood Collection System

General Hospital · 21 CFR 880.6975 · Class 2

Overview

Product CodeSIW
Device NameRobotic Peripheral Venous Blood Collection System
Regulation21 CFR 880.6975
Device ClassClass 2
Review PanelGeneral Hospital

Identification

The Aletta® Autonomous Robotic Phlebotomy Device (ARPD™) (Gen1 US) is an electromechanical device intended to perform autonomous, ultrasound-guided, venipuncture and collection of blood for diagnostic purposes in adult outpatients, monitored by a trained phlebotomist. The device uses robotic systems to assist with the blood collection procedure, including vessel identification, targeting, and/or needle insertion, and may perform its functions in an automated or autonomous manner.

Classification Rationale

FDA has determined that the device can be classified in Class II with the establishment of special controls for class II. FDA believes that class II (special) controls provide reasonable assurance of the safety and effectiveness of the device type.

Recent Cleared Devices (1 of 1)

RecordDevice NameApplicantDecision DateDecision
DEN250046Aletta® Autonomous Robotic Phlebotomy Device (ARPD™) (Gen1 US)VitestroAug 19, 2026DENG

Top Applicants

Innolitics

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