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FDA 510(k)

HEARTRAK AF

K-Number: K071130 · 2008-05-14

ApplicantUniversal Medical, Inc.
Decision Date2008-05-14
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEARTRAK AF is the device name listed in this FDA 510(k) record. The listed applicant is Universal Medical, Inc.. It received FDA 510(k) clearance on 2008-05-14 under 510(k) number K071130. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEARTRAK AF?

HEARTRAK AF is a medical device that received FDA 510(k) clearance on 2008-05-14. The listed applicant is Universal Medical, Inc.. The 510(k) number is K071130.

When did HEARTRAK AF receive FDA 510(k) clearance?

HEARTRAK AF received FDA 510(k) clearance on 2008-05-14, under 510(k) number K071130.

Who is the listed applicant for HEARTRAK AF?

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

What is the FDA product code for HEARTRAK AF?

The FDA product code for HEARTRAK AF is DXH. This falls under the Hematology category.

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Other records listing Universal Medical, 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.

K083535HEARTRAK SMART ECATK033451HEARTRAK SMART AT/HEARTRAK SMART2K980624CARDIOSTATIONK960499HEARTRAK XLK954495PACETRAK PLUSK943123PACETRAK

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Related Devices (Code: DXH)

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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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