FDA.report

510(k) K920769

Device
KONICA LI 10 AND 10A LASER IMAGER
Applicant
KONICA CORP.
510(k) number
K920769
Product code
LMC  
Decision
Substantially Equivalent (SESE)
Decision date
1992-05-06
Date received
1992-02-06
Regulation
892.2040
Classification name
Camera, Multi Format, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
RUSSELL D MUNVES
Address
9 E. 37th St. New York NY US 10016 10016

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Other 510(k) Records For Product Code LMC  

510(k)DeviceApplicantDecision date
K141454SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MDSony Electronics, Inc.2014-06-26
K141346SONY HYBIRD GRAPHIC UP-971AD, SONY HYBIRD GRAPHIC PRINTER UP-991ADSony Electronics, Inc.2014-06-26
K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.2011-10-06
K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.2009-10-16
K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.2009-05-22
K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.2009-01-09
K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.2008-07-01
K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation2007-10-25
K061999DRY LASER IMAGER, DRYPRO MODEL 832Konica Minolta Medical & Graphic, Inc.2006-08-15
K061302DIGITAL PRINTER P6000D SERIES, MODEL P6000DUMitsubishi Electric Corporation Kyoto Works2006-06-23
K060440CODONICS HORIZON XL DIGITAL DIRECT LONG FILM IMAGER; CODONICS HORIZON XL-X LONG FILM IMAGERCodonics, Inc.2006-03-16
K052251DRYSTAR MODEL 5500Agfa Corporation2005-08-31
K042133DRY LASER IMAGER, MODEL DRYPRO MODEL 793Konica Minolta Medical & Graphic, Inc.2004-11-24
K042232NP-2600 SERIES HARDCOPY PRINTERSCodonics, Inc.2004-10-05
K042158KODAK MEDICAL IMAGER 300Eastman Kodak Company2004-09-24

Legacy Summary

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FDA Review

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