510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072008Substantially Equivalent

Braemar Er900 Wireless Series Arrhythmia Event Recorder

Braemar Manufacturing, LLC, Eagan MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K072008 is the FDA 510(k) clearance record for BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER, a class II device, cleared for Braemar, Inc. on under FDA product code DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency). FDA records list 13 510(k) clearances for BRAEMAR MANUFACTURING, LLC, from to . As of , FDA records show 2 recalls naming K072008.

Clearance record

Decision date
Received
(72 days to decision)
Product code
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation
21 CFR 870.2910
Device class
Class II
Review panel
Cardiovascular
Applicant
Braemar, Inc. 1285 Corporate Center Dr., Eagan MN
510(k) summary
Statement
Third party review
No

Clearances, product code DRG

Trailing 12 months
2 clearances under product code DRG in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260