ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE— 510(k) K896540

Name: FDA 510(k) clearance K896540
Creator: U.S. Food and Drug Administration
Published: 1990-04-19

Substantially Equivalent

Nuclear Data Systems

FDA 510(k) clearance K896540 for ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE, Substantially Equivalent on 1990-04-19. Applicant: Nuclear Data Systems. Device class: 1.

Clearance details

Applicant: Nuclear Data Systems
Product code: Code IZD
Device class: Class 1
Regulation: 21 CFR 892.1320
Advisory panel: Radiology
Date received: 1989-11-15
Decision date: 1990-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Schaumburg, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZD

view all

K133781 — DECLIPSESPECT LAPAROSCOPY2014-04-11
K123917 — DECLIPSESPECT VIEWER2013-01-25
K101887 — CONFIDENT SURGERY SUITE 300, MODEL CSS3002011-03-22
K013751 — HANDHELD GAMMA FINDER (HGF)2002-02-06
K983768 — MODIFICATION TO GAMMA GUIDANCE SYSTEM1999-07-02

More clearances from Nuclear Data Systems

view all

K925650 — IMAGEVIEW 50001993-09-14

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