SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEM


Device Classification Name

instrument, biopsy

510(k) Number K021137
Device Name SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEM
Original Applicant
SANARUS MEDICAL, INC.
5880 west las positas,suite 52
pleasanton, 
CA 
94588

Original Contact vicent cutarelli
Regulation Number 876.1075
Classification Product Code
KNW  
Date Received 04/09/2002
Decision Date 06/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No