MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM


Device Classification Name

unit, electrosurgical, endoscopic (with or without accessories)

510(k) Number K030315
Device Name MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM
Original Applicant
ULTROID, LLC
2230 damon rd.
carson city, 
NV 
89701

Original Contact ronald r newton
Regulation Number 876.4300
Classification Product Code
KNS  
Date Received 01/30/2003
Decision Date 02/27/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

Gastroenterology/Urology

statement

statement

Type Special
Reviewed by Third Party No

Combination Product

No