LUMAPROBE


Device Classification Name

powered laser surgical instrument

510(k) Number K073000
Device Name LUMAPROBE
Applicant
CLAREBLEND, INC.
675 pine street
elgin, 
IL 
60123

Applicant Contact jill creasy
Correspondent
CLAREBLEND, INC.
675 pine street
elgin, 
IL 
60123

Correspodent Contact jill creasy
Regulation Number 878.4810
Classification Product Code
GEX  
Subsequent Product Code
ILY  
Date Received 10/24/2007
Decision Date 10/01/2008
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