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NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K885149
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1989
Days to Decision
42 days

NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K885149
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1989
Days to Decision
42 days