Vortran Medical Technology 1, Inc.
Vortran Medical Technology 1, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2021, with 2 FDA device recalls on record.
Top product codes for Vortran Medical Technology 1, Inc.
FDA recalls by Vortran Medical Technology 1, Inc.
- Z-2092-2017 — VORTRAN Automatic Resuscitator, VARPlus with Extension Kit; Model PCE-5012; Qty: 10 each. Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure cycled ventilatory support.
- Z-2091-2017 — VORTRAN Automatic Resuscitator, VARPlus; Model PTE-5002; Qty: 10 each Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure cycled ventilatory support.
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 Vortran Medical Technology 1, Inc.
- K202219 — VORTRAN GO2VENT with PEEP Valve
- K182292 — VORTRAN APM-Plus
- K173914 — VORTRAN Cuff Inflator (VCI)
- K162968 — VORTRAN GO2VENT
- K153733 — VORTRAN Manometer
- K103639 — VORTRAN AIRWAY PRESSURE MONITOR (VAPM)-ADULT, VORTRAN AIRWAY PRESSURE MONITOR (VAPM)- PEDIATRIC
- K073261 — VAR MONITOR
- K041473 — VAR-PLUS (VORTRAN AUTOMATIC RESUSCITATOR), MODEL PCM
- K003684 — PERCUSSIVENEB, MODEL PN-2001
- K001430 — RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000
- K982016 — PIPER IPPB MODEL 2055
- K981726 — PERCUSSIVETECH HF, MODEL 2001
- K973975 — RESPIRTECHPRO
- K963910 — HEART NEBULIZER #100609
- K943600 — UNIHEART
- K944643 — AUTONEB ACCESSORY CROSS (AAC)
- K935693 — AUTONEB BREATH ACTUATED CONTROLLER AND ACCESSORY KIT
- K933915 — VENTI-GENTLE-HALER(TM)
- K924667 — AEROSOL CHARGING ADAPTOR (FOR USE W/MININEB ONLY)
- K924649 — SOFT-MIST(TM)
- K923596 — HEART NEBULIZER
- K920443 — MININEB
- K920332 — HEART NUBULIZER
- K911759 — VORTRAN INTERMITTENT SIGNAL ACTIVATED NEBULIZER
- K896696 — (HEART) NEBULIZER
- K873477 — INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)
- K842988 — VMT GENTLE-HALER
- K841894 — VMT HAND HELD NEBULIZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.