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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
K772070VENTILATOR SETUP, VOLUMENovember 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
K772069VOL. VENTILATOR SETUP W/OUT NEBULIZERNovember 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
K760080CANNULA, NASAL, FOR OXYGENJuly 15, 1976
K760081FILTER, BACTERIA (#2290)July 15, 1976