← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

NQJ — Catheter, Hemodialysis, Non-Implanted, Ultrafiltration, For Peripheral Use

Dual lumen, non-implanted, peripheral access catheters are inserted in the peripheral arm vein and are indicated for temporary (up to 8 hours) ultrafiltration treatment of patients with fluid overload.

DEVICE CLASS
Class II
REGULATION
21 CFR 876.5540
MEDICAL SPECIALTY
Gastroenterology, Urology
REVIEW PANEL
GU
— Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
1
510(K)/PMA CLEARANCES
510k: 1
0
RECALL ENTRIES

Recent clearances

K252226Nuwellis, Inc. · 510k2025-08-13

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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