MINOLTA PULSOX-2


Device Classification Name

oximeter

510(k) Number K021469
Device Name MINOLTA PULSOX-2
Original Applicant
KONICA MINOLTA SENSING, INC.
2703 josephine st.
denver, 
CO 
80205

Original Contact nanci dexter
Regulation Number 870.2700
Classification Product Code
DQA  
Date Received 05/07/2002
Decision Date 02/12/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No