Class Class II

Purema H Hemoconcentrator – Pediatric (K243920)

K243920 2025-09-19 Traditional
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Description

Purema H Hemoconcentrator - Pediatric by Medica USA, Inc., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243920
Clearance Date2025-09-19
Clearance TypeTraditional
Product CodeKDI
Regulation Number876.5860

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