DIGIRAD REUSABLE IMAGE MEDIA— 510(k) K854407

Substantially Equivalent

Digirad Corp.

FDA 510(k) clearance K854407 for DIGIRAD REUSABLE IMAGE MEDIA, Substantially Equivalent on 1986-03-10. Applicant: Digirad Corp.. Device class: 1.

Clearance details

Applicant: Digirad Corp.
Product code: Code LQA
Device class: Class 1
Regulation: 21 CFR 892.1840
Advisory panel: Radiology
Date received: 1985-11-01
Decision date: 1986-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

More clearances from Digirad Corp.

K123408 — ERGO IMAGING SYSTEM2013-01-15
K100838 — ERGO IMAGING SYSTEM2010-04-23
K083649 — CARDIUS 3 X-ACT2009-03-09
K082904 — STASYS MOTION CORRECTION SOFTWARE2008-12-17
K082368 — CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM2008-09-12

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