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NOETIX, BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K893992
510(k) Type
Traditional
Applicant
NOETIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1989
Days to Decision
95 days

NOETIX, BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K893992
510(k) Type
Traditional
Applicant
NOETIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1989
Days to Decision
95 days