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FDA 510(k)

AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR

K-Number: K813522 · 1982-04-01

ApplicantVitar
Decision Date1982-04-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR is the device name listed in this FDA 510(k) record. The listed applicant is Vitar. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K813522. 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 AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR?

AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Vitar. The 510(k) number is K813522.

When did AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR receive FDA 510(k) clearance?

AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR received FDA 510(k) clearance on 1982-04-01, under 510(k) number K813522.

Who is the listed applicant for AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR?

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

What is the FDA product code for AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR?

The FDA product code for AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR is DXN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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