FDA 510(k) Applications Submitted by SKYTRON, DIV. THE KMW GROUP, INC.

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.
K071698 06/21/2007 AURORA LED SERIES SURGICAL LIGHTS SKYTRON, DIV. THE KMW GROUP, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact