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GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K833352
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1983
Days to Decision
36 days

GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K833352
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1983
Days to Decision
36 days