Viterion Telehealthcare, LLC
Viterion Telehealthcare, LLC holds FDA 510(k) medical device clearance, cleared in 2003, with 3 FDA device recalls on record.
Top product codes for Viterion Telehealthcare, LLC
FDA recalls by Viterion Telehealthcare, LLC
- Z-0820-2013 — Viterion TeleHealth Monitor Model Number V100, Product Codes 09377512 (US) and 04480218 (UK). Physiological patient monitor (without arrhythmia detection or alarms). Viterion V100, V100-BGM and V500 Telehealth Monitors transfer medical information.
- Z-0821-2013 — Viterion TeleHealth Monitor Model Number V100-BGM, Product Code 81842478 (US) -- Physiological patient monitor (without arrhythmia detection or alarms) . Viterion V100, V100-BGM and V500 Telehealth Monitors transfer medical information.
- Z-0822-2013 — Viterion TeleHealth Monitor Model Number V500; Product Codes 08832984 (US) and 02080468 (UK) - Physiological patient monitor (without arrhythmia detection or alarms). Viterion V100, V100-BGM and V500 Telehealth Monitors transfer medical information.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Viterion Telehealthcare, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.