Class Class II

Utepreva Endometrial Sampler (UP01) (K240595)

K240595 2024-08-14 Traditional
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Description

Utepreva Endometrial Sampler (UP01) by Utepreva, LLC — FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240595
Clearance Date2024-08-14
Clearance TypeTraditional
Product CodeHFE
Regulation Number884.1100

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