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510(k) K896739

KONICA KFDR-S by Konica Medical Corp. — Product Code LMA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 30, 1990
Date Received
November 30, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Digitizer, Image, Radiological
Device Class
Class II
Regulation Number
892.2030
Review Panel
RA
Submission Type

Other clearances by Konica Medical Corp.

  • K990969 — KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSOR (June 18, 1999)
  • K963913 — MD100 & MM150 (October 8, 1997)
  • K963914 — CM & CM DS-7 (October 8, 1997)
  • K955583 — VIFS (May 14, 1996)
  • K931316 — KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSOR (December 14, 1993)
  • K933830 — KONICA LD-4500 LASER DIGITIZER (December 14, 1993)
  • K931315 — KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSOR (December 14, 1993)
  • K931317 — KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSOR (December 14, 1993)
  • K931312 — KONICA SRX-101 AUTOMATIC X-RAY FILM PROCESSOR (September 7, 1993)
  • K931314 — KONICA QX-70 AUTOMATIC X-RAY FILM PROCESSOR (September 7, 1993)

Other clearances for product code LMA

  • K132183 — DICOM VIDEO (October 3, 2013)
  • K130636 — TELERADPRO EDGE; TELERADPRO EDGE HD-CCD (June 7, 2013)
  • K130406 — DIAGNOSTICPRO EDGE (April 29, 2013)
  • K102476 — TELERADPRO (October 7, 2010)
  • K093809 — VIDAR DENTAL FILM DIGITIZER (January 7, 2010)
  • K091288 — MEDI-6000 MEDICAL IMAGE DIGITIZER (August 14, 2009)
  • K063424 — FILM DIGITZER, MODEL 2908 MAMMO PRO (December 21, 2006)
  • K042484 — NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER (October 20, 2004)
  • K033637 — MEDICAL IMAGE DIGITIZER, MODEL 2908 (December 17, 2003)
  • K032022 — DIGITAL IMAGER (September 2, 2003)