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RAPITEX(R) RF NEW

Page Type
Cleared 510(K)
510(k) Number
K903852
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1990
Days to Decision
9 days

RAPITEX(R) RF NEW

Page Type
Cleared 510(K)
510(k) Number
K903852
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1990
Days to Decision
9 days