SIDEPORT PINCH CLAMP DEVICE


Device Classification Name

set, administration, intravascular

510(k) Number K010888
Device Name SIDEPORT PINCH CLAMP DEVICE
Original Applicant
MEDIVICE SYSTEMS, LTD.
beit hapa’amon (box 124)
20 hata’as st.
kfar saba, 

IL

44425

Original Contact ahava stein
Regulation Number 880.5440
Classification Product Code
FPA  
Date Received 03/23/2001
Decision Date 06/27/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

Type Traditional
Reviewed by Third Party No

Combination Product

No