Truecare Biomedix Intravascular Administration Set, Truecare Biomedix Extension Set

FDA 510(k) K111351 · Us Infusion Dba Truecare Biomedix

Substantially Equivalent

510(k) numberK111351

Submission

Device name
Truecare Biomedix Intravascular Administration Set, Truecare Biomedix Extension Set
Applicant
Us Infusion Dba Truecare Biomedix
Miami, FL, US
Received
May 13, 2011
Decision date
September 29, 2011
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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Questions and answers

When was Truecare Biomedix Intravascular Administration Set, Truecare Biomedix Extension Set cleared by the FDA?

Truecare Biomedix Intravascular Administration Set, Truecare Biomedix Extension Set (K111351) received a 510(k) decision of Substantially Equivalent on September 29, 2011, 139 days after the submission was received.

What is the product code of K111351?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.