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FDA 510(k)

DL900 SERIES HOLTER RECORDER

K-Number: K071733 · 2007-07-24

ApplicantBraemar, Inc.
Decision Date2007-07-24
Product CodeMWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DL900 SERIES HOLTER 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 2007-07-24 under 510(k) number K071733. 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 DL900 SERIES HOLTER RECORDER?

DL900 SERIES HOLTER RECORDER is a medical device that received FDA 510(k) clearance on 2007-07-24. The listed applicant is Braemar, Inc.. The 510(k) number is K071733.

When did DL900 SERIES HOLTER RECORDER receive FDA 510(k) clearance?

DL900 SERIES HOLTER RECORDER received FDA 510(k) clearance on 2007-07-24, under 510(k) number K071733.

Who is the listed applicant for DL900 SERIES HOLTER 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 DL900 SERIES HOLTER RECORDER?

The FDA product code for DL900 SERIES HOLTER 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 RECORDERK071011MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDERK042469BRAEMAR ER800 SERIES ENHANCED ALGORITHM 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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