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BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES

Page Type
Cleared 510(K)
510(k) Number
K895725
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1989
Days to Decision
42 days

BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES

Page Type
Cleared 510(K)
510(k) Number
K895725
510(k) Type
Traditional
Applicant
INTERSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1989
Days to Decision
42 days