Class Class II

Spectra S1 Pro; Spectra S2 Pro (K251423)

K251423 2026-02-06 Traditional
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Description

Spectra S1 Pro; Spectra S2 Pro by Uzinmedicare Co., Ltd., an FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251423
Clearance Date2026-02-06
Clearance TypeTraditional
Product CodeHGX
Regulation Number884.5160

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