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MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A

Page Type
Cleared 510(K)
510(k) Number
K875179
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1988
Days to Decision
277 days

MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A

Page Type
Cleared 510(K)
510(k) Number
K875179
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1988
Days to Decision
277 days