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LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2

Page Type
Cleared 510(K)
510(k) Number
K896515
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
90 days

LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2

Page Type
Cleared 510(K)
510(k) Number
K896515
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
90 days