CONCENTRIC BALLOON GUIDE CATHETER, MODEL 90072


Device Classification Name

catheter, percutaneous

510(k) Number K021899
Device Name CONCENTRIC BALLOON GUIDE CATHETER, MODEL 90072
Original Applicant
CONCENTRIC MEDICAL, INC.
2585 leghorn st.
mountain view, 
CA 
94043

Original Contact kevin macdonald
Regulation Number 870.1250
Classification Product Code
DQY  
Date Received 06/10/2002
Decision Date 07/10/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls