DIGIRAD 2020TC SPECT IMAGING SYSTEM— 510(k) K982855

Name: FDA 510(k) clearance K982855
Creator: U.S. Food and Drug Administration
Published: 1998-11-04

Substantially Equivalent

Digirad Corp.

FDA 510(k) clearance K982855 for DIGIRAD 2020TC SPECT IMAGING SYSTEM, Substantially Equivalent on 1998-11-04. Applicant: Digirad Corp.. Device class: 2.

Clearance details

Applicant: Digirad Corp.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1998-08-06
Decision date: 1998-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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