CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR
K-Number: K071995 · 2007-12-18
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Device Summary
Frequently Asked Questions
What is the CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR?
CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR is a medical device that received FDA 510(k) clearance on 2007-12-18. The listed applicant is Card Guard Scientific Survival , Ltd.. The 510(k) number is K071995.
When did CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR receive FDA 510(k) clearance?
CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR received FDA 510(k) clearance on 2007-12-18, under 510(k) number K071995.
Who is the listed applicant for CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR?
The FDA 510(k) record lists Card Guard Scientific Survival , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR?
The FDA product code for CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR is DSI.
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 Card Guard Scientific Survival , Ltd. 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: DSI)
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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