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AUTOMATED BIOPSY DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K913815
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1991
Days to Decision
65 days
Submission Type
Statement

AUTOMATED BIOPSY DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K913815
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1991
Days to Decision
65 days
Submission Type
Statement