Konica Minolta Medical & Graphic, Inc.
Konica Minolta Medical & Graphic, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2013.
Top product codes for Konica Minolta Medical & Graphic, Inc.
Recent clearances by Konica Minolta Medical & Graphic, Inc.
- K130936 — AERODR SYSTEM WITH P-31
- K123499 — AEROPILOT
- K120752 — AERODR STITCHING SYSTEM
- K121109 — AERODR X70
- K120477 — AEROSYNC FOR AERODR SYSTEM
- K120131 — REGIUS SIGMA2
- K113248 — AERODR SYSTEM WITH P-21
- K110717 — KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM
- K103703 — REGUIS SIGMA
- K101842 — ACIES
- K102349 — AERODR SYSTEM
- K092717 — DIRECT DIGITIZER, REGIUS MODEL 210
- K081637 — LASER IMAGER DRYPRO MODEL 873
- K071436 — REGIUS UNITEA
- K071181 — DIRECT DIGITIZER, REGIUS MODEL 110
- K061999 — DRY LASER IMAGER, DRYPRO MODEL 832
- K053173 — DS CASSETTE
- K051998 — REGIUS MODEL 170 DIRECT DIGITIZER
- K052095 — MODIFICATION TO: DIRECT DIGITIZER REGIUS MODEL 190
- K051523 — REGIUS CONSOLE CS-2000 AND REGIUS CONSOLE CS-3000, MEDICAL IMAGE PROCESSING WORKSTATION
- K051418 — DIRECT DIGITIZER REGIUS MODEL 370
- K051521 — REGIUS RS-1000, MEDICAL IMAGE PROCESSING WORKSTATION
- K042386 — DIRECT DIGITIZER, REGIUS MODEL 190
- K042133 — DRY LASER IMAGER, MODEL DRYPRO MODEL 793
- K023061 — KONICA DIRECT DIGITIZER REGIUS, MODEL 170
- K013054 — KONICA DIRECT DIGITIZER REGIUS MODEL 350
- K013052 — KONICA LASER IMAGER, DRYPRO MODEL 751/752
Data sourced from openFDA. This site is unofficial and independent of the FDA.