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BLOOD FLOW ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K820959
510(k) Type
Traditional
Applicant
BIOFAX MEDICAL INSTRUMENTATION CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1982
Days to Decision
49 days

BLOOD FLOW ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K820959
510(k) Type
Traditional
Applicant
BIOFAX MEDICAL INSTRUMENTATION CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1982
Days to Decision
49 days