PHLEBOTEST 2000


Device Classification Name

plethysmograph, photoelectric, pneumatic or hydraulic

510(k) Number K022047
Device Name PHLEBOTEST 2000
Original Applicant
OSBORN MEDICAL CORP.
100 west main
utica, 
MN 
55979

Original Contact bill davis
Regulation Number 870.2780
Classification Product Code
JOM  
Date Received 06/24/2002
Decision Date 11/04/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No