510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Inspiron Corp.

Mchenry, IL, US

Inspiron Corp. appears in FDA device records in Mchenry, IL. FDA records list 20 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
20
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 20 510(k) clearances for Inspiron Corp. between 1976 and 1986. The busiest year on record is 1976, with 7. The most recent is 1986, with 1.

Clearances by year, as a table
510(k) clearance decisions for Inspiron Corp., by decision year
YearClearances
19767
19776
19845
19851
19861
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K860838INSPIRON DOUBLE SWIVEL TRACH ADAPTERBZASubstantially Equivalent
K850346OXYGEN CONCENTRATORCAWSubstantially Equivalent
K843932VAPOR-PHASE HUMIDIFIER SYS-ADVANCEDBTTSubstantially Equivalent
K840935MANUAL RESUSCITATION SYSTEMBTMSubstantially Equivalent
K841158NEBULO 28 NEBULIZER KITBTTSubstantially Equivalent
K840418INSPIRATORY/EXPIRATORY MUSCLE EXERCISBWFSubstantially Equivalent
K834290INSPIRON LIQUID OXYGEN SYSTEMBYJSubstantially Equivalent
K772072MANIFOLD & NEBU. FOR DOUB. LINE MACH.CAFSubstantially Equivalent
K772071MANIFOLD & NEBU. FOR SINGLE LINE MACH.CAFSubstantially Equivalent
K772070VENTILATOR SETUP, VOLUMECAFSubstantially Equivalent
K772069VOL. VENTILATOR SETUP W/OUT NEBULIZERBZOSubstantially Equivalent
K772068MANIFOLD & NEBULIZER, UNIVERSALCAFSubstantially Equivalent
K770549PEDIATRIC ANESTHESIA CIRCUITCAISubstantially Equivalent
K760891INSPIRON I.M.V. SET UPCBOSubstantially Equivalent
K760461NOSE CLIPBXJSubstantially Equivalent
K760313KIT, PREP, INSPIRON IVKZDSubstantially Equivalent
K760082BOTTLE, CONDENSATE (#1628)CBCSubstantially Equivalent
K760037HEATER, IMMERSION W/ HUMIDIFIER & NEBUL.BTTSubstantially Equivalent
K760081FILTER, BACTERIA (#2290)CAHSubstantially Equivalent
K760080CANNULA, NASAL, FOR OXYGENCATSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain