FDA clears Konted C10 series pocket ultrasound system

The FDA has cleared the Konted C10 series pocket ultrasound system (C10MTpro, C10MXpro, C10MSpro, C10MBpro, C10MRpro) via 510(k) pathway for diagnostic imaging.

• The clearance covers models C10MTpro, C10MXpro, C10MSpro, C10MBpro, and C10MRpro.
• Device classified under FDA product code IYN (ultrasonic pulsed echo imaging system).

Automated summary

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