PRECISEPLAN 2.0


Device Classification Name

system,planning,radiation therapy treatment

510(k) Number K022411
Device Name PRECISEPLAN 2.0
Original Applicant
PRECISION THERAPY INTL., INC.
3155 northwoods pkwy nw
norcross, 
GA 
30071

Original Contact peter stegagno
Regulation Number 892.5050
Classification Product Code
MUJ  
Date Received 07/24/2002
Decision Date 09/20/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls