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FDA 510(k)

NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT

K-Number: K082599 · 2008-10-17

ApplicantCnsystem Medizintechnik AG
Decision Date2008-10-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT is the device name listed in this FDA 510(k) record. The listed applicant is Cnsystem Medizintechnik AG. It received FDA 510(k) clearance on 2008-10-17 under 510(k) number K082599. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT?

NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT is a medical device that received FDA 510(k) clearance on 2008-10-17. The listed applicant is Cnsystem Medizintechnik AG. The 510(k) number is K082599.

When did NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT receive FDA 510(k) clearance?

NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT received FDA 510(k) clearance on 2008-10-17, under 510(k) number K082599.

Who is the listed applicant for NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT?

The FDA 510(k) record lists Cnsystem Medizintechnik AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT?

The FDA product code for NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT is DXN.

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Related Devices (Code: DXN)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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