Corventis, Inc.
Corventis, Inc. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2014.
Top product codes for Corventis, Inc.
Recent clearances by Corventis, Inc.
- K133701 — NUVANT MCT SYSTEM
- K113372 — NUVANT, MOBILC CARDIAC TELEMETRY
- K113187 — AVIVO MOBILE PATIENT MANAGEMENT
- K111917 — NUVANT, MOBILE CARDIAC TELEMETRY
- K091971 — AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM
- K090696 — NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM
- K083287 — AVIVO MOBILE PATIENT MANAGEMENT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.