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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