Braemar Manufacturing, LLC
Braemar Manufacturing, LLC holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2018, with 3 FDA device recalls on record.
Top product codes for Braemar Manufacturing, LLC
FDA recalls by Braemar Manufacturing, LLC
- Z-0708-2025 — Monitoring Service Application (MSA). Software to process, analyze, display, and report cardiac events in ECG data received from compatible devices.
- Z-1460-2020 — Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
- Z-1459-2020 — Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Braemar Manufacturing, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.