Inspiron Corp.
Inspiron Corp. appears in FDA public data with 0 recalls, 20 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 9, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 20
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K860838 | INSPIRON DOUBLE SWIVEL TRACH ADAPTER | April 9, 1986 |
| K850346 | OXYGEN CONCENTRATOR | February 4, 1985 |
| K843932 | VAPOR-PHASE HUMIDIFIER SYS-ADVANCED | October 18, 1984 |
| K840935 | MANUAL RESUSCITATION SYSTEM | April 5, 1984 |
| K841158 | NEBULO 28 NEBULIZER KIT | March 30, 1984 |
| K840418 | INSPIRATORY/EXPIRATORY MUSCLE EXERCIS | February 17, 1984 |
| K834290 | INSPIRON LIQUID OXYGEN SYSTEM | February 4, 1984 |
| K772068 | MANIFOLD & NEBULIZER, UNIVERSAL | November 15, 1977 |
| K772071 | MANIFOLD & NEBU. FOR SINGLE LINE MACH. | November 15, 1977 |
| K772070 | VENTILATOR SETUP, VOLUME | November 15, 1977 |
| K772069 | VOL. VENTILATOR SETUP W/OUT NEBULIZER | November 15, 1977 |
| K772072 | MANIFOLD & NEBU. FOR DOUB. LINE MACH. | November 15, 1977 |
| K770549 | PEDIATRIC ANESTHESIA CIRCUIT | March 30, 1977 |
| K760891 | INSPIRON I.M.V. SET UP | December 9, 1976 |
| K760461 | NOSE CLIP | August 26, 1976 |
| K760313 | KIT, PREP, INSPIRON IV | August 4, 1976 |
| K760082 | BOTTLE, CONDENSATE (#1628) | July 16, 1976 |
| K760037 | HEATER, IMMERSION W/ HUMIDIFIER & NEBUL. | July 16, 1976 |
| K760080 | CANNULA, NASAL, FOR OXYGEN | July 15, 1976 |
| K760081 | FILTER, BACTERIA (#2290) | July 15, 1976 |