Class Class II

Avicenna Roboflex (K233700)

K233700 2024-08-16 Traditional
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Description

Avicenna Roboflex by Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233700
Clearance Date2024-08-16
Clearance TypeTraditional
Product CodeFGB
Regulation Number876.1500

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