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FDA 510(k)

BLOOD PRESSURE MONITORING DEVICES

K-Number: K822614 · 1982-09-21

Decision Date1982-09-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITORING DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 1982-09-21 under 510(k) number K822614. 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 BLOOD PRESSURE MONITORING DEVICES?

BLOOD PRESSURE MONITORING DEVICES is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K822614.

When did BLOOD PRESSURE MONITORING DEVICES receive FDA 510(k) clearance?

BLOOD PRESSURE MONITORING DEVICES received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822614.

Who is the listed applicant for BLOOD PRESSURE MONITORING DEVICES?

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

What is the FDA product code for BLOOD PRESSURE MONITORING DEVICES?

The FDA product code for BLOOD PRESSURE MONITORING DEVICES 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.

Other records listing Allied Healthcare Products, Inc. as applicant

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.

View all 24 devices →

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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