STELLAR


Device Classification Name

light, surgical, ceiling mounted

510(k) Number K002463
Device Name STELLAR
Original Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
5000 36th st s.e.
p.o.box 888615
grand rapids, 
MI 
49588 -8615

Original Contact kari ogreen
Regulation Number 878.4580
Classification Product Code
FSY  
Date Received 08/10/2000
Decision Date 11/08/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No