← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
QBP — Cap, Device Disinfectant
Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time
DEVICE CLASS
Class II
REGULATION
21 CFR 880.5440
MEDICAL SPECIALTY
General Hospital
REVIEW PANEL
HO
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
2
510(K)/PMA CLEARANCES
510k: 2
0
RECALL ENTRIES
Recent clearances
K252006Icu Medical, Inc. · 510k2026-03-27
K2515921World Vista Medical · 510k2026-02-11
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.
Weekly Briefing
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.