510(k) K210036

Carnation Ambulatory Monitor (CAM) by Bardy Diagnostics, Inc. — Product Code DSH

K210036 is an FDA 510(k) premarket notification submitted by Bardy Diagnostics, Inc. for the device "Carnation Ambulatory Monitor (CAM)". The FDA issued a decision of Substantially Equivalent on February 5, 2021. The device falls under product code DSH (Recorder, Magnetic Tape, Medical), a Class II device regulated under 21 CFR 870.2800. Bardy Diagnostics, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 2021
Date Received
January 6, 2021
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Recorder, Magnetic Tape, Medical
Device Class
Class II
Regulation Number
870.2800
Review Panel
CV
Submission Type