FDA 510(k) Applications Submitted by MAX LINDERT

FDA 510(k) Number Submission Date Device Name Applicant
K000976 03/27/2000 DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM) INSTRUMENTARIUM IMAGING, INC.
K001171 04/11/2000 DELTA 16 TACT INSTRUMENTARIUM IMAGING, INC.
K981641 05/08/1998 MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQ INSTRUMENTARIUM CORP.


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