MODIFICATION TO HP M2376A DEVICE LINK SYSTEM


codes

Device Classification Name

monitor,physiological,patient(without arrhythmia detection or alarms)

510(k) Number K000635
Device Name MODIFICATION TO HP M2376A DEVICE LINK SYSTEM
Original Applicant
AGILENT TECHNOLOGIES, INC.
3000 minuteman rd.
andover, 
MA 
01810 -1099

Original Contact mike hudon
Regulation Number 870.2300
Classification Product Code
MWI  
Date Received 02/25/2000
Decision Date 03/20/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Special
Reviewed by Third Party No

Combination Product

No