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RADI-BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K850605
510(k) Type
Traditional
Applicant
RADIPLAST AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1985
Days to Decision
175 days

RADI-BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K850605
510(k) Type
Traditional
Applicant
RADIPLAST AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1985
Days to Decision
175 days