Hmd Biomedical, Inc.
Hmd Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2022.
Top product codes for Hmd Biomedical, Inc.
Recent clearances by Hmd Biomedical, Inc.
- K212248 — GlucoLeader Enhance 2 Blood Glucose Monitoring System
- K182428 — GlucoLeader Enhance Blood Glucose Monitoring System
- K140150 — Goodlife AC-300 Blood Glucose Monitoring System, Goodlife AC-301 Blood Glucose Monitoring System, Goodlife AC-302 Blood Glucose Monitoring System, Goodlife AC 303 Blood Glucose Monitoring System, Goodlife AC-304 Blood Glucose Monitoring System Goodlife AC-305 Blood Glucose Monitoring System, Goodlife AC-300 Professional Blood Glucose Monitoring System, Goodlife AC-301 Professional Blood Glucose Monitoring System Goodlife AC-30
- K131173 — FIA Blood Glucose Monitoring System (G2)
- K121433 — GOODLIFE CS-200 (SINGLE PATIENT USE), CS-200 PROFESSIONAL (MULTIPLE PATIENT USE) BLOOD GLUCOSE MONITORING SYSTEMS
- K113314 — PRECICHEK NS-101 POCT PROFESSIONAL BLOOD GLUCOSE MONITORING SYSTEM
- K120064 — TEST, BLOOD GLUCOSE SYSTEM
- K113307 — GL GOODLIFE SERIES BLOOD GLUCOSE MONITORING SYSMTEM
- K032985 — GLUCOLEADER ENHANCE SELF-MONITORING OF BLOOD GLUCOSE SYSTEM
- K023279 — GLUCOLEADER VALUE
Data sourced from openFDA. This site is unofficial and independent of the FDA.