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FDA 510(k)

RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE

K-Number: K896777 · 1990-02-27

ApplicantResearch Medical, Inc.
Decision Date1990-02-27
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1990-02-27 under 510(k) number K896777. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE?

RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Research Medical, Inc.. The 510(k) number is K896777.

When did RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE receive FDA 510(k) clearance?

RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE received FDA 510(k) clearance on 1990-02-27, under 510(k) number K896777.

Who is the listed applicant for RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE?

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

What is the FDA product code for RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE?

The FDA product code for RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE is DWF.

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Related Devices (Code: DWF)

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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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