SENORX ES-300


Device Classification Name

electrosurgical, cutting & coagulation & accessories

510(k) Number K030473
Device Name SENORX ES-300
Applicant
SENORX, INC.
11 columbia, suite a
aliso viejo, 
CA 
92656

Applicant Contact amy boucly
Regulation Number 878.4400
Classification Product Code
GEI  
Date Received 02/12/2003
Decision Date 02/26/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No