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Assert-IQ - Assert-IQ (DM5000)
FDA 510(k)Class II (US FDA 510(k))
510(k) K251221
by Abbott
Identifiers
- 510(k) Number
- K251221 FDA 510(k)
- FDA Product Code
- MXD FDA 510(k)
- Models / Variants
- Assert-IQ (DM5000) FDA 510(k)Assert-IQ (DM5300) FDA 510(k)Assert-IQ (DM5500) FDA 510(k)Merlin.net (MN7000) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1025 FDA 510(k)
- Regulation Number
- 870.1025 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Assert-IQ - Assert-IQ (DM5000) by Abbott — Class II — FDA_510K — listed in FDA 510(k) — 4 models — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K251221 | Class II | Active |
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Manufacturer
- Manufacturer
- Abbott
Sources (1)
- FDA 510(k) K251221 24 fields · synced Jun 18, 2026