CRYOPROBE


Device Classification Name

unit, cryosurgical, accessories

510(k) Number K024009
Device Name CRYOPROBE
Original Applicant
H&O EQUIPMENTS NV/SA
4655 kirkwood ct.
boulder, 
CO 
80301

Original Contact lewis ward
Regulation Number 878.4350
Classification Product Code
GEH  
Date Received 12/04/2002
Decision Date 03/20/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No