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SKYTRON INFINITY SERIES SURGICAL LIGHTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915285
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1992
Days to Decision
87 days
Submission Type
Statement

SKYTRON INFINITY SERIES SURGICAL LIGHTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915285
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1992
Days to Decision
87 days
Submission Type
Statement