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INTELLIVUE PATIENT MONITOR, MODELS MP2, MP5, MP20, MP30, MP40, MP50, MO60, MP7-, MP80, AND MP90

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083517
510(k) Type
Special
Applicant
Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
51 days
Submission Type
Summary

INTELLIVUE PATIENT MONITOR, MODELS MP2, MP5, MP20, MP30, MP40, MP50, MO60, MP7-, MP80, AND MP90

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083517
510(k) Type
Special
Applicant
Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
51 days
Submission Type
Summary