Spectral Diagnostics, Inc.
Spectral Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2006.
Top product codes for Spectral Diagnostics, Inc.
Recent clearances by Spectral Diagnostics, Inc.
- K052519 — SPECTRAL WEST NILE VIRUS IGM STATUS TEST
- DEN030002 — ENDOTOXIN ACTIVITY ASSAY (EAA) DEVICE
- K030057 — SPECTRAL CARDIAC STATUS CK-MB/MYOGLOBIN/TROPONIN I 3-IN-1 TEST
- K022409 — SPECTRAL'S CARDIAC STATUS CK-MB RAPID TEST
- K020950 — SPECTRAL'S 2 IN 1 (TNI-MYO)
- K014105 — SPECTRAL'S TROPONIN I
- K992127 — CARDIOQUANT TROPONIN I TEST
- K991447 — CARDIOQUANT CARDIAC ASSESSMENT CONTROLS
- K982679 — MULTIQUANT (R) QUANTITATIVE MYOGLOBIN TEST
- K981474 — CARDIAC STATUS CONTROLS (CK-MB/MYOGLOBIN/TROPONIN I)
- K972687 — CARDIAC STATUS CONTROLS/TROPONIN I
- K972408 — CARDIAC STATUS CONTROLS
Data sourced from openFDA. This site is unofficial and independent of the FDA.