CATHETER CONNECTIONS' DUALCAP SOLO

Cap, Device Disinfectant

CATHETER CONNECTIONS, INC.

The following data is part of a premarket notification filed by Catheter Connections, Inc. with the FDA for Catheter Connections' Dualcap Solo.

Pre-market Notification Details

Device IDK113842
510k NumberK113842
Device Name:CATHETER CONNECTIONS' DUALCAP SOLO
ClassificationCap, Device Disinfectant
Applicant CATHETER CONNECTIONS, INC. 2455 E Parleys Way - Suite 150 Salt Lake City,  UT  84109
ContactDonald D Solomon
CorrespondentDonald D Solomon
CATHETER CONNECTIONS, INC. 2455 E Parleys Way - Suite 150 Salt Lake City,  UT  84109
Product CodeQBP  
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-12-28
Decision Date2012-01-27
Summary:summary

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