FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Corvair Monza

K Number: K252589 · Decision Jan 9, 2026
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
424
Applicant Total
19
Review Days
147

Basic Information

Device Name
Corvair Monza
K Number
K252589
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AliveCor, Inc.
Date Received
August 15, 2025
Decision Date
January 9, 2026
Product Code
MHX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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Other Clearances by AliveCor, Inc.

K Number Device Name
K231010 Corvair
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K212662 AliveCor QT Service
K211668 KardiaMobile Card
K210753 KardiaMobile 6L
K201985 KardiaAI
K191406 KardiaMobile, KardiaStation
K183319 Triangle System
K182396 KardiaMobile, KardiaStation
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