Inspiron Corp.
FDA 510(k) medical device clearances.
Top product codes for Inspiron Corp.
Recent clearances by Inspiron Corp.
- K860838 — INSPIRON DOUBLE SWIVEL TRACH ADAPTER
- K850346 — OXYGEN CONCENTRATOR
- K843932 — VAPOR-PHASE HUMIDIFIER SYS-ADVANCED
- K840935 — MANUAL RESUSCITATION SYSTEM
- K841158 — NEBULO 28 NEBULIZER KIT
- K840418 — INSPIRATORY/EXPIRATORY MUSCLE EXERCIS
- K834290 — INSPIRON LIQUID OXYGEN SYSTEM
- K772068 — MANIFOLD & NEBULIZER, UNIVERSAL
- K772069 — VOL. VENTILATOR SETUP W/OUT NEBULIZER
- K772070 — VENTILATOR SETUP, VOLUME
- K772071 — MANIFOLD & NEBU. FOR SINGLE LINE MACH.
- K772072 — MANIFOLD & NEBU. FOR DOUB. LINE MACH.
- K770549 — PEDIATRIC ANESTHESIA CIRCUIT
- K760891 — INSPIRON I.M.V. SET UP
- K760461 — NOSE CLIP
- K760313 — KIT, PREP, INSPIRON IV
- K760037 — HEATER, IMMERSION W/ HUMIDIFIER & NEBUL.
- K760082 — BOTTLE, CONDENSATE (#1628)
- K760080 — CANNULA, NASAL, FOR OXYGEN
- K760081 — FILTER, BACTERIA (#2290)
Data sourced from openFDA. This site is unofficial and independent of the FDA.