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MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT MONITORS, BLOOD ANALYSIS PORTAL SYSTEM PLUG-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013624
510(k) Type
Special
Applicant
Philips Medizin Systeme Boblingen GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2001
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT MONITORS, BLOOD ANALYSIS PORTAL SYSTEM PLUG-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013624
510(k) Type
Special
Applicant
Philips Medizin Systeme Boblingen GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2001
Days to Decision
28 days
Submission Type
Summary