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FDA PRODUCT CODE · CLASS II

JCX — Apparatus, Suction, Ward Use, Portable, Ac-Powered

DEVICE CLASS
Class II
REGULATION
21 CFR 878.4780
MEDICAL SPECIALTY
General, Plastic Surgery
REVIEW PANEL
SU
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
4
510(K)/PMA CLEARANCES
510k: 4
0
RECALL ENTRIES

Recent clearances

K250964Jiangsu Jumao X-Care Medical Equipment Co., Ltd. · 510k2026-05-11
K243638Microvention · 510k2025-06-13
K251111Excitus AS · 510k2025-05-07
K243418Micro Therapeutics, Inc. d/b/a ev3 Neurovascular · 510k2024-12-02

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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