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FDA 510(k)

MRL BLOOD PRESSURE MONITOR

K-Number: K885191 · 1989-05-23

ApplicantMedical Research Laboratories, Inc.
Decision Date1989-05-23
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MRL BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Research Laboratories, Inc.. It received FDA 510(k) clearance on 1989-05-23 under 510(k) number K885191. 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 MRL BLOOD PRESSURE MONITOR?

MRL BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K885191.

When did MRL BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

MRL BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1989-05-23, under 510(k) number K885191.

Who is the listed applicant for MRL BLOOD PRESSURE MONITOR?

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

What is the FDA product code for MRL BLOOD PRESSURE MONITOR?

The FDA product code for MRL BLOOD PRESSURE MONITOR is DXN.

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Other records listing Medical Research Laboratories, Inc. as applicant

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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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