FDA 510(k), K061771, EZ-CONNECT

510(K) Number: K061771
Device Name: EZ-CONNECT
Manufacturer: VIDACARE CORPORATION
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 06/23/2006
Decision Date: 07/10/2006
Regulation Medical Specialty: General Hospital

Total pages: 58
Fully redacted pages: 5
Content pages: 53