L1 SYSTEM


Device Classification Name

lancet, blood

510(k) Number K024170
Device Name L1 SYSTEM
Original Applicant
PELIKAN TECHNOLOGIES, INC
1072 east meadow circle
palo alto, 
CA 
94303

Original Contact jack green
Regulation Number 878.4800
Classification Product Code
FMK  
Date Received 12/18/2002
Decision Date 04/14/2003
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