FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IIVS INTEGRATED IMAGE VIEWING STATION

K Number: K994329 · Decision May 26, 2000
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
14
Review Days
156

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
IIVS INTEGRATED IMAGE VIEWING STATION
K Number
K994329
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terarecon,Inc.
Date Received
December 22, 1999
Decision Date
May 26, 2000
Product Code
LMD
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LMD System, Digital Image Communications, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LMD), ordered by most recent decision date.

View all

Other Clearances by Terarecon,Inc.

K Number Device Name
K250288 TeraRecon Cardiovascular.Calcification.CT
K243158 TeraRecon Aorta.CT (1.1.0)
K241312 TeraRecon Cardiac.Chambers.MR (1.0.0)
K220349 TeraRecon Neuro
K200750 Neuro.Al Algorithm
K191585 iNtuition-Structural Heart Module
K180916 iNtuition-T1 Mapping and T2/T2* Mapping
K131447 INTUITION - TDA, TVA, PARAMETRIC MAPPING
K121916 INTUITION
K061214 AQUARIUSAPS SERVER
Search all 14 clearances from Terarecon,Inc. →