MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY


Device Classification Name

instrument, biopsy

510(k) Number K022879
Device Name MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
Original Applicant
SANARUS MEDICAL, INC.
5880 west las positas,suite 52
pleasanton, 
CA 
94588

Original Contact vincent cutarelli
Regulation Number 876.1075
Classification Product Code
KNW  
Date Received 08/30/2002
Decision Date 09/23/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

General & Plastic Surgery

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls