MEDGRAPHIX INTL VR 1000 SERIES— 510(k) K921381

Name: FDA 510(k) clearance K921381
Creator: U.S. Food and Drug Administration
Published: 1992-11-02

Substantially Equivalent

Medgraphix Intl.

FDA 510(k) clearance K921381 for MEDGRAPHIX INTL VR 1000 SERIES, Substantially Equivalent on 1992-11-02. Applicant: Medgraphix Intl.. Device class: 2.

Clearance details

Applicant: Medgraphix Intl.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1992-03-23
Decision date: 1992-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rosemont, PA, 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

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