Hypoguard USA, Inc.
Hypoguard USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2006.
Top product codes for Hypoguard USA, Inc.
Recent clearances by Hypoguard USA, Inc.
- K053079 — ASSURE PRO BLOOD GLUCOSE MONITORING SYSTEM, MODEL 460001
- K051514 — ASSURE PRO BLOOD GLUCOSE MONITORING SYSTEM, MODEL 460002
- K041881 — ADVANCE MICRO-DRAW BLOOD GLUCOSE MONITORING SYSTEM, MODEL 411100
- K033851 — DIASCREEN REAGENT STRIPS FOR URINALYSIS, MODELS D122OO (2GK), D12100 (1K), D11100 (1G)
- K031388 — MODIFICATION TO HYPOGUARD ADVANCE BLOOD GLUCOSE MONITORING SYSTEM
- K024347 — EXPRESS BLOOD GLUCOSE MONITORING SYSTEM
- K022545 — GLUCOBALANCE DATA MANAGEMENT SOFTWARE, MODEL 555020
- K020232 — HYPOGUARD ADVANCE BLOOD GLUCOSE MONITORING SYSTEM
- K010973 — DIASCREEN 50 URINE CHEMISTRY ANALYZER, MODEL # 1242-00; DIASCREEN REAGENT STRIP FOR URINALYSIS, CAT. # D11000
Data sourced from openFDA. This site is unofficial and independent of the FDA.