510(k) K142097

SELEC-3 I.V.ADMINISTRATION SET by Biomedix, Inc. — Product Code FPA

K142097 is an FDA 510(k) premarket notification submitted by Biomedix, Inc. for the device "SELEC-3 I.V.ADMINISTRATION SET". The FDA issued a decision of Substantially Equivalent on August 29, 2014. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Biomedix, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 2014
Date Received
August 1, 2014
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type