BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER— 510(k) K945130

Name: FDA 510(k) clearance K945130
Creator: U.S. Food and Drug Administration
Published: 1995-04-12

Substantially Equivalent

Braemar Corp.

FDA 510(k) clearance K945130 for BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER, Substantially Equivalent on 1995-04-12. Applicant: Braemar Corp.. Device class: 2.

Clearance details

Applicant: Braemar Corp.
Product code: Code DSH
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 1994-10-19
Decision date: 1995-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burnsville, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DSH

product code DSH

Death: 3
Injury: 652
Total: 655

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.