Dia Imaging Analysis, Ltd.

Dia Imaging Analysis, Ltd. holds 10 FDA 510(k) medical device clearances, first cleared 2020, most recent 2025.

Top product codes for Dia Imaging Analysis, Ltd.

QIH — Radiology10 devices

Recent clearances by Dia Imaging Analysis, Ltd.

K243862 — LVivo Software ApplicationCode QIH·2025-03-17
K243331 — LVivo SeamlessCode QIH·2025-03-06
K243235 — LVivo Software ApplicationCode QIH·2025-03-03
K240553 — LVivo Software ApplicationCode QIH·2024-10-04
K240769 — LVivo IQSCode QIH·2024-05-24
K222970 — LVivo IQSCode QIH·2023-02-01
K212466 — LVivo SeamlessCode QIH·2021-12-09
K210053 — LVivo Software ApplicationCode QIH·2021-02-05
K202546 — LVivo SeamlessCode QIH·2020-09-29
K200232 — LVivo Software ApplicationCode QIH·2020-06-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.