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 | Device Class | Medical Specialty |
|---|---|---|---|
| MXD | Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection) | FDA class 2 | Cardiovascular |
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