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FDA 510(k)

HEARTRAK SMART ECAT

K-Number: K083535 · 2008-12-15

Decision Date2008-12-15
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEARTRAK SMART ECAT 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 2008-12-15 under 510(k) number K083535. 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 SMART ECAT?

HEARTRAK SMART ECAT is a medical device that received FDA 510(k) clearance on 2008-12-15. The listed applicant is Universal Medical, Inc.. The 510(k) number is K083535.

When did HEARTRAK SMART ECAT receive FDA 510(k) clearance?

HEARTRAK SMART ECAT received FDA 510(k) clearance on 2008-12-15, under 510(k) number K083535.

Who is the listed applicant for HEARTRAK SMART ECAT?

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 SMART ECAT?

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

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 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.

View all 8 devices →

Related Devices (Code: DXH)

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

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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