SENOCOR 360 CIRCUMFERENTIAL VACUUM ASSISTED BIOPSY DEVICE, 8 GAUGE


Device Classification Name

instrument, biopsy

510(k) Number K023923
Device Name SENOCOR 360 CIRCUMFERENTIAL VACUUM ASSISTED BIOPSY DEVICE, 8 GAUGE
Original Applicant
SENORX, INC.
11 columbia, suite a
aliso viejo, 
CA 
92656

Original Contact amy boucly
Regulation Number 876.1075
Classification Product Code
KNW  
Date Received 11/25/2002
Decision Date 12/11/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

General & Plastic Surgery

statement

statement

Type Special
Reviewed by Third Party No

Combination Product

No