AUTO BOX DL 6200 767215

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 1996-11-22 for AUTO BOX DL 6200 767215 manufactured by Sensormedics Corp..

Event Text Entries

[17481453] In the model 6200, a capacitor on the co2 analyzer assembly burned up. There were no injuries and no pt involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2050001-1996-00032
MDR Report Key53658
Report Source05,06,07
Date Received1996-11-22
Date of Report1996-11-20
Date of Event1996-11-01
Date Mfgr Received1996-11-01
Device Manufacturer Date1996-02-01
Date Added to Maude1996-12-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAUTO BOX DL
Generic NameBODY PLETHYSMOGRAPH
Product CodeJEH
Date Received1996-11-22
Returned To Mfg1996-11-08
Model Number6200
Catalog Number767215
Lot NumberNA
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key54257
ManufacturerSENSORMEDICS CORP.
Manufacturer Address22705 SAVI RANCH PARKWAY YORBA LINDA CA 928874645 US
Baseline Brand NameAUTOBOX DL
Baseline Generic NameBODY PLETHYSMOGRAPH
Baseline Model No6200
Baseline Catalog No767215
Baseline IDNA
Baseline Device FamilyNA
Baseline Shelf Life ContainedA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK923989
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1996-11-22

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