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Gtimd, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K202433Aqueduct 200 Cervical Dilation Balloon CatheterOctober 15, 2021
K202427Aqueduct 100 Plus Cervical Dilation Balloon CatheterNovember 6, 2020
K160664Aqueduct 100 Cervical DilatorAugust 1, 2016