Last synced on 14 November 2025 at 11:06 pm

LASERFLO BLOOD PERFUSION MONITOR 403

Page Type
Cleared 510(K)
510(k) Number
K851057
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1985
Days to Decision
102 days

LASERFLO BLOOD PERFUSION MONITOR 403

Page Type
Cleared 510(K)
510(k) Number
K851057
510(k) Type
Traditional
Applicant
TSI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1985
Days to Decision
102 days