Class Class II

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle (K222852)

K222852 2023-05-25 Traditional
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Description

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle by Nipro Medical Corporation — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222852
Clearance Date2023-05-25
Clearance TypeTraditional
Product CodeFMI
Regulation Number880.5570

Categories

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