Non-Pvc Fluid Path Port Access Infusion Set (with and Without Injection Set)

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K974829 ↗

FDA Product Code

LJT

Device Class

Class II

Regulation

21 CFR Part 880.5965

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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See all devices from Kawasumi Laboratories Co., Ltd. →