DeviceClearance

Product code QBP— General Hospital

CUROS PORT PROTECTOR

Classification name
Cap, Device Disinfectant
Device class
Class 2
Regulation
21 CFR 880.5440
Advisory panel
General Hospital
Total cleared
22
First cleared
Most recent

FDA classification definition

“Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time”

— U.S. Food and Drug Administration, device classification record for product code QBP under 21 CFR 880.5440, via openFDA

Market context for product code QBP

FDA has cleared 22 devices under product code QBP between 2008 and 2026, filed by 13 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code QBP

Recent clearances under product code QBP

Data sourced from openFDA. This site is unofficial and independent of the FDA.