Vitalograph Ireland, Ltd.

FDA Regulatory Profile

Vitalograph Ireland, Ltd. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 25, 2023.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Known Names

vitalograph (ireland), vitalograph ireland

Recent 510(k) Clearances

K-NumberDeviceDate
K223818Model 9160 VitaloQUBMay 25, 2023
K221030Model 9100 PFT/DICOJuly 15, 2022
K212938Vitalograph Model 6000 AlphaJanuary 26, 2022
K201562SpirotracOctober 14, 2020
K200550Vitalograph Model 2120 In2itive eDiaryJuly 27, 2020