Cirrus Diagnostics, Inc.
Cirrus Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1992.
Top product codes for Cirrus Diagnostics, Inc.
Recent clearances by Cirrus Diagnostics, Inc.
- K921704 — IMMULITE(R) FSH
- K920411 — IMMULITE HLH
- K914833 — IMMULITE DIGOXIN
- K911796 — IMMULITE(TM) HCG
- K910677 — IMMULITE(TM) T-UPTAKE
- K910261 — IMMULITE(TM) TOTAL T4
- K905648 — CRP LIPID REAGENT TEST PACK
- K905214 — IMMULITE (TM) TOTAL T3
- K905769 — IMMULITE HS-TSH
- K905215 — IMMULITE (TM) AUTOMATED IMMUNOASSAY ANALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.