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FDA 510(k) Applications Submitted by Dr. Heinz-Werner Henke
FDA 510(k) Number
Submission Date
Device Name
Applicant
K222462
08/15/2022
Semi-automatic Biopsy-Needle (BIM 18/20); Semi-automatic Biopsy-Needle (BIM 18.15); Semi-automatic Biopsy-Needle (BIM 18/10);Semi-automatic Biopsy-Needle (BIM 16/20);Semi-automatic Biopsy-Needle (BIM 16/15);Semi-automatic Biopsy-Needle (BIM 16/10);Semi-au
ITP Innovative Tomography Products GmbH
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