CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED


Device Classification Name

set, administration, intravascular

510(k) Number K072576
Device Name CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED
Applicant
BAXTER HEALTHCARE CORP.
1620 waukegan rd.
mpgr-al
mcgaw park, 
IL 
60085

Applicant Contact nanette hedden
Correspondent
BAXTER HEALTHCARE CORP.
1620 waukegan rd.
mpgr-al
mcgaw park, 
IL 
60085

Correspodent Contact nanette hedden
Regulation Number 880.5440
Classification Product Code
FPA  
Date Received 09/13/2007
Decision Date 11/06/2007
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No