510(k) K130975

SWABCAP AND SWABFLUSH by Excelsior Medical Corp. — Product Code QBP

K130975 is an FDA 510(k) premarket notification submitted by Excelsior Medical Corp. for the device "SWABCAP AND SWABFLUSH". The FDA issued a decision of Substantially Equivalent on December 24, 2013. The device falls under product code QBP (Cap, Device Disinfectant), a Class II device regulated under 21 CFR 880.5440. Excelsior Medical Corp. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 24, 2013
Date Received
April 8, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cap, Device Disinfectant
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type

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