← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
PND — Midline Catheter
The catheter is inserted into the peripheral vascular system for infusion of fluids and medications for less than 28 days.
DEVICE CLASS
Class II
REGULATION
21 CFR 880.5200
MEDICAL SPECIALTY
General Hospital
REVIEW PANEL
HO
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
1
510(K)/PMA CLEARANCES
510k: 1
0
RECALL ENTRIES
Recent clearances
K252402Terumo Medical Products (Hangzhou) Co., Ltd. · 510k2025-12-18
Related on SPEQ
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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