KONICA LI 10 AND 10A LASER IMAGER— 510(k) K920769

Substantially Equivalent

Konica Corp.

FDA 510(k) clearance K920769 for KONICA LI 10 AND 10A LASER IMAGER, Substantially Equivalent on 1992-05-06. Applicant: Konica Corp.. Device class: 2.

Clearance details

Applicant: Konica Corp.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1992-02-06
Decision date: 1992-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMC

K141346 — SONY HYBIRD GRAPHIC UP-971AD, SONY HYBIRD GRAPHIC PRINTER UP-991AD2014-06-26
K141454 — SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD2014-06-26
K111566 — DRYVIEW CHROMA IMAGING SYSTEM2011-10-06
K092280 — CYPHER DICOM PRINT SOLUTION2009-10-16
K090469 — CARESTREAM DRYVIEW 5850 LASER IMAGER2009-05-22

More clearances from Konica Corp.

K992586 — KONICA LASER IMAGER, DRYPRO MODEL 7221999-10-29
K990359 — KONICA DIRECT DIGITIZER, MODEL DD-3411999-08-17
K980873 — KONICA DIRECT DIGITIZER REGIUS MODEL 3301998-06-19
K920558 — KONICA DIRECT DIGITIZER KD-10001992-03-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.