KONICA LASER IMAGER LI-21— 510(k) K950359

Name: FDA 510(k) clearance K950359
Creator: U.S. Food and Drug Administration
Published: 1995-09-06

Substantially Equivalent

Storch Amini & Munves PC

FDA 510(k) clearance K950359 for KONICA LASER IMAGER LI-21, Substantially Equivalent on 1995-09-06. Applicant: Storch Amini & Munves PC. Device class: 2.

Clearance details

Applicant: Storch Amini & Munves PC
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1995-01-27
Decision date: 1995-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMC

view all

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 Storch Amini & Munves PC

view all

K950358 — KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR1995-03-17

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