Medical Device Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT, INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR, INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
46
Total
46
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medical Device Technologies, Inc. General Hospital ✕
2 devices