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

Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000)

K Number: K251221 · Decision Sep 17, 2025
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
32
Applicant Total
12
Review Days
149

Basic Information

Device Name
Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000)
K Number
K251221
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott
Date Received
April 21, 2025
Decision Date
September 17, 2025
Product Code
MXD
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
MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)

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