PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES


information about

Device Classification Name

syringe, piston

510(k) Number K002381
Device Name PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES
Original Applicant
PENTAFERTE S.R.L.
zona industriale
campli, teramo, 

IT

64012

Original Contact vittorio servidori
Regulation Number 880.5860
Classification Product Code
FMF  
Date Received 08/04/2000
Decision Date 01/11/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

Type Traditional
Reviewed by Third Party No

Combination Product

No