Vivachek Biotech (Hangzhou) Co., Ltd.
Vivachek Biotech (Hangzhou) Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2026.
Top product codes for Vivachek Biotech (Hangzhou) Co., Ltd.
Recent clearances by Vivachek Biotech (Hangzhou) Co., Ltd.
- K261280 — BioSieve Multi-Drug Urine Test Panel; BioSieve Multi-Drug Urine Home Test Panel
- K252554 — Wisdiag Multi-Drug Urine Test Cup; Wisdiag Multi-Drug Urine Home Test Cup
- K241869 — BioSieve Fentanyl FIA Home Test Kit; BioSieve Fentanyl FIA Pro Test Kit; BioSieve Toxismart Reader
- K222126 — VivaChek Fad Blood Glucose Monitoring System, VivaChek Fad Smart Blood Glucose Monitoring System, VivaChek Fad Sync Blood Glucose Monitoring System
- K240124 — BioSieve Fentanyl FIA Test Kit; BioSieve ToxiSmart FIA Reader
- K233058 — VivaChek Link Plus Blood Glucose Monitoring System
- K233062 — BioSieveTM Multi-Drug Urine Test Panel; BioSieveTM Multi-Drug Urine Test Panel Rx
- K231978 — BioSieve Marijuana Test Panel 50 +5 more
- K222667 — Wisdiag Multi-Drug Urine Test Cup, Wisdiag Multi-Drug Urine Test Cup Rx
- K192957 — VivaChek Blood Glucose and B-Ketone Monitoring System
Data sourced from openFDA. This site is unofficial and independent of the FDA.