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LUMISCOPE EMS 8000

Page Type
Cleared 510(K)
510(k) Number
K901849
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1990
Days to Decision
122 days

LUMISCOPE EMS 8000

Page Type
Cleared 510(K)
510(k) Number
K901849
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1990
Days to Decision
122 days