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FDA 510(k) Applications Submitted by KONICA MEDICAL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990969
03/23/1999
KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSOR
KONICA MEDICAL CORP.
K963913
09/30/1996
MD100 & MM150
KONICA MEDICAL CORP.
K963914
09/30/1996
CM & CM DS-7
KONICA MEDICAL CORP.
K955583
12/05/1995
VIFS
KONICA MEDICAL CORP.
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