MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER— 510(k) K844132

Name: FDA 510(k) clearance K844132
Creator: U.S. Food and Drug Administration
Published: 1985-01-22

Substantially Equivalent

Sigma Teleproducts, Inc.

FDA 510(k) clearance K844132 for MEDIVISION SERIES 5000 FLUOROSCOPIC DIGITAL IMAGER, Substantially Equivalent on 1985-01-22. Applicant: Sigma Teleproducts, Inc.. Device class: 1.

Clearance details

Applicant: Sigma Teleproducts, Inc.
Product code: Code LMB
Device class: Class 1
Regulation: 21 CFR 892.2010
Advisory panel: Radiology
Date received: 1984-10-23
Decision date: 1985-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMB

view all

K992131 — SAMSUNG RAYPAX LONG TERM ARCHIVE1999-09-13
K984405 — ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-40001999-02-08
K983447 — WISE (II) IMAGE MANAGEMENT SYSTEM1998-10-29
K980243 — PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)1998-04-03
K973463 — OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE1997-12-02

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