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Philips Medizinsysteme Boeblingen GmbH, Cardiac an

Boeblingen, Baden-Wuerttemberg, DE

Philips Medizinsysteme Boeblingen GmbH, Cardiac AN appears in FDA device records in Boeblingen, Baden-Wuerttemberg, DE. FDA records list 25 510(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
25
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 25 510(k) clearances for Philips Medizinsysteme Boeblingen GmbH, Cardiac an between 2007 and 2014. The busiest year on record is 2009, with 5. The most recent is 2014, with 2.

Clearances by year, as a table
510(k) clearance decisions for Philips Medizinsysteme Boeblingen GmbH, Cardiac an, by decision year
YearClearances
20074
20081
20095
20104
20114
20122
20133
20142
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K141015INTELLIVUE PATIENT MONITOR MX400, INTELLIVUE PATIENT MONITOR MX450, INTELLIVUE PATIENT MONITOR MX500, INTELLIVUE PATIENTMHXSubstantially Equivalent
K132320INTELLIVUE CL RESPIRATION PODBZQSubstantially Equivalent
K131872INTELLIVUE PATIENT MONITOR MX500, INTELLIVUE PATIENT MONITOR MX550MHXSubstantially Equivalent
K131829INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K130849INTELLIVUE PATIENT MONITOR MX400; INTELLIVUE PATIENT MONITOR MX450MHXSubstantially Equivalent
K120366INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K113441PHYSIOLOGICAL MONITOR, PATIENT MONITORMHXSubstantially Equivalent
K111905INTELLIVUE GUARDIAN SOFTWARE MODEL 866009, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216DXJSubstantially Equivalent
K110474PHILIPS INTELLIVUE TCG10LKDSubstantially Equivalent
K111083PHILIPS AVALON FETAL/MATERNAL MONITORS FM20, FM30, FM40 AND FM50HGMSubstantially Equivalent
K110622INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K101600INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216, INTELLIVUE PATIENT MONITORS MP5, MP2, X2 MODELDQASubstantially Equivalent
K101449INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K093268INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K100939INTELLIVUE PATIENT MONITOR MODEL: MP2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP75, MP80 AND MP90MHXSubstantially Equivalent
K091927INTELLIVUE PATIENT MONITORS ,MODELS MP40, MP50, MP60, MP70, MP80, MP90DSISubstantially Equivalent
K091572DISPOSABLE SPO2 SENSOR M1134ADQASubstantially Equivalent
K091395MP5 INTELLIVUE PATIENT MONITORMHXSubstantially Equivalent
K082583INTELLIVUE PATIENT MONITOR, INTELLIBRIDGE MODULE, MODELS MP40, MP50, MP60, MP70, MP80, MP90, EC10, EC5MHXSubstantially Equivalent
K083517INTELLIVUE PATIENT MONITOR, MODELS MP2, MP5, MP20, MP30, MP40, MP50, MO60, MP7-, MP80, AND MP90DSISubstantially Equivalent
K082633INTELLIVUE PATIENT MONITOR, INTELLIVUE XDS, MODELS MP2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90DSISubstantially Equivalent
K071800PHILIPS AVALON FETAL MONITORS FM20 AND FM30HGMSubstantially Equivalent
K072070PHILIPS MP2 AND X2 INTELLIVUE PATIENT MONITORSMHXSubstantially Equivalent
K071426MP2, X2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, AND MP90 INTELLIVUE PATIENT MONITORSMHXSubstantially Equivalent
K063725MP5 INTELLIVUE PATIENT MONITORMHXSubstantially 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