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PHILIPS AVALON FETAL MONITORS FM20, FM30, FM40, AND FM50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092028
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
226 days
Submission Type
Summary

PHILIPS AVALON FETAL MONITORS FM20, FM30, FM40, AND FM50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092028
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
226 days
Submission Type
Summary