510(k) K231010

Device
Corvair
Applicant
AliveCor, Inc.
510(k) number
K231010
Product code
MHX
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-07
Date received
2023-04-07
Regulation
870.1025
Classification name
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Samip Shah
Address
189 N. Bernardo Ave. Mountain View CA US 94043 94043

FDA Registration Numbers

Source Documents

510(k) summary PDF

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