FDA 510(k) K150407, BioFlo Midline Catheter, by Navilyst Medical, Inc.

510(K) Number: K150407
Device Name: BioFlo Midline Catheter
Manufacturer: Navilyst Medical, Inc.
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 02/18/2015
Decision Date: 05/15/2015
Regulation Medical Specialty: General Hospital