Class Class II

V-SPERM WASH (K223117)

K223117 2023-01-31 Traditional
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Description

V-SPERM WASH by Vitromed GmbH — FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223117
Clearance Date2023-01-31
Clearance TypeTraditional
Product CodeMQL
Regulation Number884.6180

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