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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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