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MODIFIED LASERFLO BLOOD PERFUSION MONITOR

Page Type
Cleared 510(K)
510(k) Number
K864259
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1987
Days to Decision
114 days

MODIFIED LASERFLO BLOOD PERFUSION MONITOR

Page Type
Cleared 510(K)
510(k) Number
K864259
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1987
Days to Decision
114 days