Class Class II

Avicenna Roboflex (K233700)

K233700 2024-08-16 Traditional
Home/ Devices/ Avicenna Roboflex (K233700)

Description

Avicenna Roboflex by Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi, an 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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