Class Class II

Spectra Platinum (K251932)

K251932 2025-11-25 Traditional
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Description

Spectra Platinum by Uzinmedicare Co., Ltd., an FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251932
Clearance Date2025-11-25
Clearance TypeTraditional
Product CodeHGX
Regulation Number884.5160

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