Vitalograph (Ireland) , Ltd.
Vitalograph (Ireland) , Ltd. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2023.
Name variants for Vitalograph (Ireland) , Ltd.
as filed with FDA- Vitalograph (Ireland) , Ltd.
- Vitalograph Ireland, Ltd.
Top product codes for Vitalograph (Ireland) , Ltd.
Recent clearances by Vitalograph (Ireland) , Ltd.
- K223818 — Model 9160 VitaloQUB
- K221030 — Model 9100 PFT/DICO
- K212938 — Vitalograph Model 6000 Alpha
- K201562 — Spirotrac
- K200550 — Vitalograph Model 2120 In2itive eDiary
- K160253 — Vitalograph Model 6300 micro
- K142642 — Vitalograph Model 6600 Compact
- K142812 — Vitalograph Model 6800 Pneumotrac
- K141546 — VITALOGRAPH MODEL 7000 SPIROTRAC
- K110525 — VITALOGRAPH MODEL 7100 - VITALOJAK
- K100687 — VITALOGRAPH HAND HELD SPIROMETER, MODEL 2120
- K073155 — VITALOGRAPH MODEL 4000 (ASMA-1 AND COPD-6)
Data sourced from openFDA. This site is unofficial and independent of the FDA.