510(k) K963861

LASERSHARE PRINT SPOOLER AND/OR SOFTWARE by Dejarnette Research Systems — Product Code LMD

K963861 is an FDA 510(k) premarket notification submitted by Dejarnette Research Systems for the device "LASERSHARE PRINT SPOOLER AND/OR SOFTWARE". The FDA issued a decision of Substantially Equivalent on Dec 18, 1996. The device falls under product code LMD (System, Digital Image Communications, Radiological), a Class I device regulated under 21 CFR 892.2020. Dejarnette Research Systems has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 18, 1996
Date Received
Sep 24, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Digital Image Communications, Radiological
Device Class
Class I
Regulation Number
892.2020
Review Panel
RA
Submission Type

A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol. It may provide simple image review software functionality for medical image processing and manipulation, such as grayscale window and level, zoom and pan, user delineated geometric measurements, compression, or user added image annotations. The device does not perform advanced image processing or complex quantitative functions.