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FDA 510(k)

PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

K-Number: K874917 · 1988-05-10

ApplicantOxford Medilog, Inc.
Decision Date1988-05-10
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1988-05-10 under 510(k) number K874917. 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 PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM?

PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-05-10. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K874917.

When did PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?

PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 1988-05-10, under 510(k) number K874917.

Who is the listed applicant for PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM?

The FDA 510(k) record lists Oxford Medilog, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM?

The FDA product code for PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM is DXN.

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Related Devices (Code: DXN)

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Official Source

View on FDA Database →

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

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