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DOPPLER FLOW METER, LASER

Page Type
Cleared 510(K)
510(k) Number
K827818
510(k) Type
Traditional
Applicant
ATL INTERSPEC CARDIOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1982
Days to Decision
29 days

DOPPLER FLOW METER, LASER

Page Type
Cleared 510(K)
510(k) Number
K827818
510(k) Type
Traditional
Applicant
ATL INTERSPEC CARDIOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1982
Days to Decision
29 days