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BONE BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K001132
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2000
Days to Decision
21 days
Submission Type
Statement

BONE BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K001132
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2000
Days to Decision
21 days
Submission Type
Statement