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AURORA LED SERIES SURGICAL LIGHTS

Page Type
Cleared 510(K)
510(k) Number
K071698
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2007
Days to Decision
15 days
Submission Type
Summary

AURORA LED SERIES SURGICAL LIGHTS

Page Type
Cleared 510(K)
510(k) Number
K071698
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2007
Days to Decision
15 days
Submission Type
Summary