Medical Device Manufacturer · NL , Utrecht

Vitestro - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2026

1

Total

0

Cleared

1

Denied

FDA 510(k) Regulatory Record - Vitestro General Hospital ✕

1 devices

1-1 of 1

Not Cleared Aug 19, 2026

Aletta® Autonomous Robotic Phlebotomy Device (ARPD™) (Gen1 US)

DEN250046 · SIW

General Hospital · 327d