MAGNATEK 30


Device Classification Name

oximeter

510(k) Number K991819
Device Name MAGNATEK 30
Applicant
MAGNA ADVANCED TECHNOLOGIES, INC.
7200 n.w. seventh st.
2nd floor
miami, 
FL 
33126

Applicant Contact annie velez
Correspondent
MAGNA ADVANCED TECHNOLOGIES, INC.
7200 n.w. seventh st.
2nd floor
miami, 
FL 
33126

Correspodent Contact annie velez
Regulation Number 870.2700
Classification Product Code
DQA  
Date Received 05/27/1999
Decision Date 08/19/1999
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

Type Traditional
Reviewed by Third Party No

Combination Product

No