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FDA 510(k)

ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL

K-Number: K964235 · 1999-03-02

Decision Date1999-03-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Industrielle Entwicklung Medizintechnik Und Vertri. It received FDA 510(k) clearance on 1999-03-02 under 510(k) number K964235. 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 ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL?

ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL is a medical device that received FDA 510(k) clearance on 1999-03-02. The listed applicant is Industrielle Entwicklung Medizintechnik Und Vertri. The 510(k) number is K964235.

When did ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL receive FDA 510(k) clearance?

ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL received FDA 510(k) clearance on 1999-03-02, under 510(k) number K964235.

Who is the listed applicant for ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL?

The FDA 510(k) record lists Industrielle Entwicklung Medizintechnik Und Vertri as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL?

The FDA product code for ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL 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 Industrielle Entwicklung Medizintechnik Und Vertri 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.

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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