Class Class II

ENDOFLATOR + (K250388)

K250388 2025-09-22 Traditional
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Description

ENDOFLATOR + by Karl Storz SE & CO. KG, an FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250388
Clearance Date2025-09-22
Clearance TypeTraditional
Product CodeHIF
Regulation Number884.1730

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