Inspiron Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K860838INSPIRON DOUBLE SWIVEL TRACH ADAPTERApril 9, 1986
K850346OXYGEN CONCENTRATORFebruary 4, 1985
K843932VAPOR-PHASE HUMIDIFIER SYS-ADVANCEDOctober 18, 1984
K840935MANUAL RESUSCITATION SYSTEMApril 5, 1984
K841158NEBULO 28 NEBULIZER KITMarch 30, 1984
K840418INSPIRATORY/EXPIRATORY MUSCLE EXERCISFebruary 17, 1984
K834290INSPIRON LIQUID OXYGEN SYSTEMFebruary 4, 1984
K772069VOL. VENTILATOR SETUP W/OUT NEBULIZERNovember 15, 1977
K772072MANIFOLD & NEBU. FOR DOUB. LINE MACH.November 15, 1977
K772068MANIFOLD & NEBULIZER, UNIVERSALNovember 15, 1977
K772071MANIFOLD & NEBU. FOR SINGLE LINE MACH.November 15, 1977
K772070VENTILATOR SETUP, VOLUMENovember 15, 1977
K770549PEDIATRIC ANESTHESIA CIRCUITMarch 30, 1977
K760891INSPIRON I.M.V. SET UPDecember 9, 1976
K760461NOSE CLIPAugust 26, 1976
K760313KIT, PREP, INSPIRON IVAugust 4, 1976
K760037HEATER, IMMERSION W/ HUMIDIFIER & NEBUL.July 16, 1976
K760082BOTTLE, CONDENSATE (#1628)July 16, 1976
K760081FILTER, BACTERIA (#2290)July 15, 1976
K760080CANNULA, NASAL, FOR OXYGENJuly 15, 1976