FDA 510(k) Applications Submitted by KARI OGREEN

FDA 510(k) Number Submission Date Device Name Applicant
K021585 05/14/2002 STELLAR SERIES SURGICAL LIGHTS WITH HERMES SKYTRON, DIV. THE KMW GROUP, INC.
K992090 06/21/1999 MILLENNIUM GOLD SKYTRON, DIV. THE KMW GROUP, INC.
K002463 08/10/2000 STELLAR SKYTRON, DIV. THE KMW GROUP, INC.


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