Hemocue, Inc.
Hemocue, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2004.
Top product codes for Hemocue, Inc.
Recent clearances by Hemocue, Inc.
- K041234 — HEMOCUE HEMOGLOBIN 201DM ANALYZING SYSTEM
- K041230 — CLINICAL LABORATORY ANALYZING SYSTEM
- K032203 — HEMOCUE HEMOGLOBIN 201 + SYSTEM ARTICLE 121704
- K020935 — HEMOCUE GLUCOSE 201 SYSTEM, ARTICLE NUMBER 120706
- K962415 — HEMOCUE B-GLCOSE SYSTEM
- K961312 — HEMOCUE B-HEMOGLOBIN SYSTEM
- K961311 — HEMOCUE B-GLUCOSE SYSTEM
- K943432 — HEMOCUE B-GLUCOSE SYSTEM
- K911141 — HEMOCUE(R) B-GLUCOSE MICROCUVETTE/PHOTOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.