← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

FJK — Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

DEVICE CLASS
Class II
REGULATION
21 CFR 876.5820
MEDICAL SPECIALTY
Gastroenterology, Urology
REVIEW PANEL
GU
— Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
4
510(K)/PMA CLEARANCES
510k: 4
0
RECALL ENTRIES

Recent clearances

K252423Bain Medical Equipment (Guangzhou) Co., Ltd. · 510k2026-05-15
K251341Vital Healthcare Sdn. Bhd. · 510k2026-01-16
K251442Ningbo Tianyi Medical Appliance Co., Ltd. · 510k2025-10-02
K243607Diality, Inc. · 510k2024-12-20

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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