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LASER RF TEST -RHEUMATOID FACTOR(S) REAGENTS

Page Type
Cleared 510(K)
510(k) Number
K850296
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1985
Days to Decision
78 days

LASER RF TEST -RHEUMATOID FACTOR(S) REAGENTS

Page Type
Cleared 510(K)
510(k) Number
K850296
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/1985
Days to Decision
78 days