Digirad Corp.
Digirad Corp. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2013.
Top product codes for Digirad Corp.
Recent clearances by Digirad Corp.
- K123408 — ERGO IMAGING SYSTEM
- K100838 — ERGO IMAGING SYSTEM
- K083649 — CARDIUS 3 X-ACT
- K082904 — STASYS MOTION CORRECTION SOFTWARE
- K082368 — CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM
- K070542 — CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS
- K052430 — CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM
- K051549 — CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM
- K030085 — CARDIUS-1 AND CARDIS-2
- K023110 — CEDARS-SINAI MOTION CORRECTION (MOCO) SOFTWARE, MODEL 111005
- K011572 — QUANTITATIVE GATED SPECT (QGS), QUANTITATIVE PERFUSION SPECT (QPS)
- K982855 — DIGIRAD 2020TC SPECT IMAGING SYSTEM
- K961104 — NOTEBOOK IMAGER
- K854407 — DIGIRAD REUSABLE IMAGE MEDIA
- K852284 — DIGIRAD SYSTEM 1 AND THE REUSUABLE IMAGE MEDIA
- K828562 — DIGIRAD CFR 2000 RADIOGRAPHIC FILM CASSETTE
Data sourced from openFDA. This site is unofficial and independent of the FDA.