VISISHARE IMAGING SYSTEM AND/ OR SOFTWARE, VISISHARE SYSTEM AND/ OR SOFTWARE— 510(k) K974130

Substantially Equivalent

Dejarnette Research Systems

FDA 510(k) clearance K974130 for VISISHARE IMAGING SYSTEM AND/ OR SOFTWARE, VISISHARE SYSTEM AND/ OR SOFTWARE, Substantially Equivalent on 1998-01-29. Applicant: Dejarnette Research Systems. Device class: 1.

Clearance details

Applicant
Dejarnette Research Systems
Product code
Code LMD
Device class
Class 1
Regulation
21 CFR 892.2020
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Towson, MD, US
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