Vickers America Medical Corp.
Vickers America Medical Corp. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1984.
Top product codes for Vickers America Medical Corp.
Recent clearances by Vickers America Medical Corp.
- K840823 — TREONIC C30
- K831838 — LABORATORY DATA MGMT SYSTEM SDMS
- K830748 — RESUSCITAIRE
- K830936 — TREONIC IP5
- K813239 — OXYGENAIRE NURING INCUBATOR
- K813238 — NEOCARE BABY-CONTROLLED INCUBATOR
- K811865 — VMA PEDIATRIC APNEA MATTRESS
- K810792 — NEOCARE TEMPERATURE MONITOR
- K810067 — 140 NEOCARE AIR CONTROLLED INCUBATOR
- K810571 — NEOCARE OXYGEN MONITOR
- K802251 — SP 120 SOPHISTICATE
- K801246 — OXFORD HUMAN MILK PASTEURISER
- K791645 — VICKERS MEDICAL MODEL 112 TREONIC DC2
- K791713 — VICKERS MEDICAL MODEL 130 NEAVENT-NEO
- K790936 — MODEL 114 TREONIC H150 HAEMOHEATER
- K790657 — STRETCHER TRANSIT ISOLATER #122
- K790658 — AIRCRAFT TRANSIT ISOLATOR MODEL 121
- K790945 — MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU
- K790689 — REVISED BATTERY CHARGER
- K781562 — HEMACHECK
- K781332 — PEEP/CPAP VALVE
- K781325 — MARKII VENTIMASKS
Data sourced from openFDA. This site is unofficial and independent of the FDA.