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FDA 510(k)

BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER

K-Number: K042469 · 2004-10-06

ApplicantBraemar, Inc.
Decision Date2004-10-06
Product CodeMWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Braemar, Inc.. It received FDA 510(k) clearance on 2004-10-06 under 510(k) number K042469. The device is classified under product code MWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER?

BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER is a medical device that received FDA 510(k) clearance on 2004-10-06. The listed applicant is Braemar, Inc.. The 510(k) number is K042469.

When did BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER receive FDA 510(k) clearance?

BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER received FDA 510(k) clearance on 2004-10-06, under 510(k) number K042469.

Who is the listed applicant for BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER?

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

What is the FDA product code for BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER?

The FDA product code for BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER is MWJ.

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Other records listing Braemar, 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.

K081444BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEMK072008BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDERK071733DL900 SERIES HOLTER RECORDERK071011MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDER

Related Devices (Code: MWJ)

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.

K254119Wearable ECG Recorder (YMHeart XY-12); Wearable ECG Recorder (YMHeart XY-1201); Wearable ECG Recorder (YMHeart XY-1202); Wearable ECG Recorder (YMHeart XY-1203); Wearable ECG Recorder (YMHeart XY-03); Wearable ECG Recorder (YMHeart XY-0301); Wearable ECG Recorder (YMHeart XY-0302); Wearable ECG Recorder (YMHeart XY-0303)Shenzhen Xinyan Medical Technology Co.,ltd.K253529Peerbridge COR MDx (Cor MDx)Peerbridge Health, Inc.K253562medilogFDSchiller AGK253384mobiCARE Cardiac Monitoring System (mobiCARE-MC200M, mobiCARE-MC200ML, mobiCARE-MC200M7, mobiCARE-MC200ML7)Seers Technology Co., Ltd.K252839ZywieZ3 Sensor & AdhesiveZywie, Inc.K231424HeartBeam AIMIGo(TM) SystemHeartbeam, Inc.

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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