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FDA 510(k)

BLOOD PRESSURE MONITOR, ARTERIAL

K-Number: K780128 · 1978-01-31

ApplicantApplied Medical Research
Decision Date1978-01-31
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR, ARTERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Research. It received FDA 510(k) clearance on 1978-01-31 under 510(k) number K780128. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD PRESSURE MONITOR, ARTERIAL?

BLOOD PRESSURE MONITOR, ARTERIAL is a medical device that received FDA 510(k) clearance on 1978-01-31. The listed applicant is Applied Medical Research. The 510(k) number is K780128.

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

BLOOD PRESSURE MONITOR, ARTERIAL received FDA 510(k) clearance on 1978-01-31, under 510(k) number K780128.

Who is the listed applicant for BLOOD PRESSURE MONITOR, ARTERIAL?

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

What is the FDA product code for BLOOD PRESSURE MONITOR, ARTERIAL?

The FDA product code for BLOOD PRESSURE MONITOR, ARTERIAL is DRS.

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Other records listing Applied Medical Research as applicant

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K800025DINAMAP RESEARCH MONITOR 1245K791580CEREBRAL FUNCTION MONITOR 870K791159DINAMAP MODEL 855K790322OPTIONAL ACCESSORY FOOT SWITCH MODEL 100K790328MODEL 1051, MONITORK782073DINAMAP MODELS 1160 AND 1165

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Related Devices (Code: DRS)

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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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