BD FlowSmart Set
FDA 510(k) K150059 · Becton, Dickinson Company
510(k) numberK150059
Submission
- Device name
- BD FlowSmart Set
- Applicant
- Becton, Dickinson Company
Franklin Lakes, NJ, US - Received
- January 13, 2015
- Decision date
- April 28, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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 BD FlowSmart Set cleared by the FDA?
BD FlowSmart Set (K150059) received a 510(k) decision of Substantially Equivalent on April 28, 2015, 105 days after the submission was received.
What is the product code of K150059?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.