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FDA 510(k)

MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR

K-Number: K896102 · 1990-01-18

Decision Date1990-01-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 1990-01-18 under 510(k) number K896102. 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 MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR?

MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K896102.

When did MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1990-01-18, under 510(k) number K896102.

Who is the listed applicant for MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR?

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

What is the FDA product code for MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR?

The FDA product code for MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR 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 Advanced Medical 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 14 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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