Class Class II

See-Mode Augmented Reporting Tool, Thyroid (SMART-T) (K240697)

K240697 2024-09-09 Traditional
Home/ Devices/ See-Mode Augmented Reporting Tool,…

Description

See-Mode Augmented Reporting Tool, Thyroid (SMART-T) by See-Mode Technologies Pte, Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240697
Clearance Date2024-09-09
Clearance TypeTraditional
Product CodeQDQ
Regulation Number892.2090

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top