FDA 510(k), K020530, EVANS SUB-Q, MODEL MC4206

510(K) Number: K020530
Device Name: EVANS SUB-Q, MODEL MC4206
Manufacturer: EVANS MEDICAL, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/19/2002
Decision Date: 04/29/2002
Regulation Medical Specialty: General Hospital

Total pages: 99
Fully redacted pages: 26
Content pages: 73