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FDA 510(k)

CARDIACMONITOR

K-Number: K963375 · 1997-02-28

ApplicantVision Electronics
Decision Date1997-02-28
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIACMONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vision Electronics. It received FDA 510(k) clearance on 1997-02-28 under 510(k) number K963375. 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 CARDIACMONITOR?

CARDIACMONITOR is a medical device that received FDA 510(k) clearance on 1997-02-28. The listed applicant is Vision Electronics. The 510(k) number is K963375.

When did CARDIACMONITOR receive FDA 510(k) clearance?

CARDIACMONITOR received FDA 510(k) clearance on 1997-02-28, under 510(k) number K963375.

Who is the listed applicant for CARDIACMONITOR?

The FDA 510(k) record lists Vision Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIACMONITOR?

The FDA product code for CARDIACMONITOR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vision Electronics 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.

K962937CARDIO TEAM II

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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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