QBP

Cap, Device Disinfectant

Product code
QBP
Device name
Cap, Device Disinfectant
Device class
Class 2
21 CFR
21 CFR 880.5440
Medical specialty
General Hospital
Marketing pathway
510(K)
510(k) clearances (last 3 years)
3
Summaries archived here
3 (direct download)
510(k) clearances (all years, FDA)
22 (all years; only the last 3 years are listed here)

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

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (3)

Last three years. Most recent: 2026-03-27.

NumberDecision dateApplicantDevice nameSummary
K2520062026-03-27Icu Medical, Inc.OTTO™ Disinfecting CapPDF
K2515922026-02-111World Vista MedicalSteriHub™ Disinfecting Device and Protective CoverPDF
K2239142024-04-05Cleansite Medical, Inc.ACTIV™ CapPDF

3 summaries are archived here for direct download.

Official FDA classification page: QBP
Classification and pathway per current FDA publications. Data from openFDA (CC0).